ClinGen Allele Registry
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Canonical Allele Identifier:
PA2827938348
Gene: FGFR3
HGNC
NCBI
Linked Data
ClinVar Variation Id:
16339
ClinVar RCV Id:
RCV000017745
RCV000017742
RCV000017743
RCV000017744
RCV000297175
RCV000417690
RCV000431989
RCV000420501
RCV000438171
RCV000435437
RCV000424421
RCV000763119
RCV002276554
RCV003155033
RCV003758684
RCV004532377
RCV003989294
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Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001341739.1:p.Ser249Cys
CA126380
NM_001354810.2:c.746C>G