Canonical Allele Identifier: PA2825872318
Gene: FGFR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 13300

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001138388.1:p.Asp206Ala
CA280195
NM_001144916.2:c.617A>C