Canonical Allele Identifier: PA916018609
Gene: HSD17B4 HGNC NCBI

Linked Data

ClinVar Variation Id: 555994
ClinVar RCV Id: RCV000671924
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001278957.1:p.Ala35Thr
CA360866247
NM_001292028.2:c.103G>A