Canonical Allele Identifier: PA2825825429
Gene: HSD17B13 HGNC NCBI

Linked Data

ClinVar Variation Id: 3107109
ClinVar RCV Id: RCV004404463
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001129702.1:p.Asn192Ser
CA100822931
NM_001136230.3:c.575A>G