Canonical Allele Identifier: PA2830008491
Gene: FGFR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 13285
ClinVar RCV Id: RCV000014207

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_075418.1:p.Val180_Val181del
CA10575516
NM_023029.2:c.537_542del