Canonical Allele Identifier: PA2825060893
Gene: FGFR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 13285
ClinVar RCV Id: RCV000014207

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000132.3:p.Val269_Val270del
CA10575516
NM_000141.5:c.804_809del