Canonical Allele Identifier: PA111997
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_000133.1:p.Ser249Cys
CA126380
NM_000142.5:c.746C>G