Canonical Allele Identifier: PA2825871935
Gene: FGFR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2905267
ClinVar RCV Id: RCV003756409

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001138387.1:p.Gly213Arg
CA378330447
NM_001144915.2:c.637G>C
CA378330448
NM_001144915.2:c.637G>A