Canonical Allele Identifier: PA2830005379
Gene: FGFR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2905267
ClinVar RCV Id: RCV003756409

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_075259.4:p.Gly302Arg
CA378330447
NM_022970.3:c.904G>C
CA378330448
NM_022970.3:c.904G>A