Canonical Allele Identifier: PA2826819069
Gene: HSD17B4 HGNC NCBI

Linked Data

ClinVar Variation Id: 495866
ClinVar RCV Id: RCV000763126 RCV000590157 RCV001220352 RCV002530904 RCV003987613 RCV002260650
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001278956.1:p.Arg482Cys
CA3382299
NM_001292027.2:c.1444C>T