Canonical Allele Identifier: PA126375
Gene: FGFR4 HGNC NCBI

Linked Data

ClinVar Variation Id: 16326
ClinVar RCV Id: RCV000017723 RCV001777142 RCV001196704 RCV003974837
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_998812.1:p.Gly388Arg
CA126374
NM_213647.3:c.1162G>A
CA362291427
NM_213647.3:c.1162G>C