Canonical Allele Identifier: PA658717948
Gene: HSD17B3 HGNC NCBI

Linked Data

ClinVar Variation Id: 492762
ClinVar RCV Id: RCV000581861
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000188.1:p.Leu128Ser
CA5140445
NM_000197.2:c.383T>C