Canonical Allele Identifier: PA2827050727
Gene: FGFR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 952522
ClinVar RCV Id: RCV001224644
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001307583.1:p.Val131Phe
CA378327652
NM_001320654.2:c.391G>T