Canonical Allele Identifier: PA111831
Gene: FGFR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 952522
ClinVar RCV Id: RCV001224644
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000132.3:p.Val359Phe
CA378327652
NM_000141.5:c.1075G>T