Canonical Allele Identifier: PA128692
Gene: FGFR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 29854
ClinVar RCV Id: RCV000022733
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000132.3:p.Ala337Thr
CA128691
NM_000141.5:c.1009G>A