Canonical Allele Identifier: PA280190
Gene: FGFR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 13288
ClinVar RCV Id: RCV000014211

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000132.3:p.Asp273del
CA280189
NM_000141.5:c.818_820del