Canonical Allele Identifier: PA111560
Gene: FGFR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 478046
ClinVar RCV Id: RCV000525216 RCV000762798
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000132.3:p.Gly384Arg
CA378327226
NM_000141.5:c.1150G>A
CA378327227
NM_000141.5:c.1150G>C