Canonical Allele Identifier: PA916024583
Gene: FGFR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 374818
ClinVar Variation Id: 2131381
ClinVar RCV Id: RCV003048177

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001307587.1:p.Cys342Gly
CA16043910
NM_001320658.2:c.1024T>G
CA2580082429
NM_001320658.2:c.1023_1024delinsAG