Canonical Allele Identifier: PA2825871981
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_001138387.1:p.Cys253Gly
CA16043910
NM_001144915.2:c.757T>G
CA2580082429
NM_001144915.2:c.756_757delinsAG