Canonical Allele Identifier: PA2827051144
Gene: FGFR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 13300

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001307587.1:p.Asp321Ala
CA280195
NM_001320658.2:c.962A>C