Canonical Allele Identifier: PA2827050688
Gene: FGFR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 374815
ClinVar RCV Id: RCV000415483

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001307583.1:p.Asp108Gly
CA16043913
NM_001320654.2:c.323A>G