Canonical Allele Identifier: PA2827051297
Gene: FGFR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1285493
ClinVar RCV Id: RCV001706850

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001307587.1:p.Ile652Val
CA5720605
NM_001320658.2:c.1954A>G