Canonical Allele Identifier: PA916024575
Gene: FGFR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 374816
ClinVar Variation Id: 574062
ClinVar RCV Id: RCV000695897

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001307587.1:p.Gly338Arg
CA16043912
NM_001320658.2:c.1012G>C
CA378328094
NM_001320658.2:c.1012G>A