Canonical Allele Identifier: PA2825872517
Gene: FGFR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 661397
ClinVar Variation Id: 1698211

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001138388.1:p.Lys544Asn
CA378314114
NM_001144916.2:c.1632G>T
CA378314117
NM_001144916.2:c.1632G>C