Canonical Allele Identifier: PA2827050705
Gene: FGFR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2093701
ClinVar RCV Id: RCV002996861

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001307583.1:p.Cys114del
CA378327957
NM_001320654.2:c.342C>A
CA2580082428
NM_001320654.2:c.341_343del