Canonical Allele Identifier: PA2825871979
Gene: FGFR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 13266
ClinVar RCV Id: RCV000014178 RCV000014180 RCV000014177 RCV000014179 RCV000534888 RCV001723565
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001138387.1:p.Cys253Arg
CA256745
NM_001144915.2:c.757T>C