Canonical Allele Identifier: PA2828041820
Gene: FGFR4 HGNC NCBI

Linked Data

ClinVar Variation Id: 2548332
ClinVar RCV Id: RCV004319609
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341913.1:p.Leu449Val
CA3576362
NM_001354984.2:c.1345C>G