ClinGen Allele Registry
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Canonical Allele Identifier:
PA2830008941
Gene: FGFR2
HGNC
NCBI
Linked Data
ClinVar Variation Id:
880347
ClinVar RCV Id:
RCV001108581
RCV001108583
RCV001108585
RCV001108582
RCV001108584
RCV001856447
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_075418.1:p.Asp432Gly
CA5720695
NM_023029.2:c.1295A>G