Canonical Allele Identifier: PA2825873231
Gene: FGFR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 661397
ClinVar Variation Id: 1698211

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001138390.1:p.Lys542Asn
CA378314114
NM_001144918.2:c.1626G>T
CA378314117
NM_001144918.2:c.1626G>C