Canonical Allele Identifier: PA2830008672
Gene: FGFR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 449398
ClinVar RCV Id: RCV000523700 RCV001232531
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_075418.1:p.Tyr251Cys
CA378328024
NM_023029.2:c.752A>G