Canonical Allele Identifier: PA2827051190
Gene: FGFR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1373931

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001307587.1:p.Pro413Leu
CA5720813
NM_001320658.2:c.1238C>T