Canonical Allele Identifier: PA2825872987
Gene: FGFR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 13288
ClinVar RCV Id: RCV000014211

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001138390.1:p.Asp158del
CA280189
NM_001144918.2:c.473_475del