Canonical Allele Identifier: PA2830008631
Gene: FGFR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 29854
ClinVar RCV Id: RCV000022733

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_075418.1:p.Ala248Thr
CA128691
NM_023029.2:c.742G>A