Canonical Allele Identifier: PA2830372839
Gene: HSD17B13 HGNC NCBI

Linked Data

ClinVar Variation Id: 3107109
ClinVar RCV Id: RCV004404463
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_835236.2:p.Asn228Ser
CA100822931
NM_178135.5:c.683A>G