Canonical Allele Identifier: PA2825873032
Gene: FGFR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2977031
ClinVar RCV Id: RCV003831149

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001138390.1:p.Asp206Glu
CA378328471
NM_001144918.2:c.618C>G
CA378328473
NM_001144918.2:c.618C>A