Canonical Allele Identifier: PA916024553
Gene: FGFR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 13276

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001307583.1:p.Gln61Pro
CA280178
NM_001320654.2:c.182A>C