Canonical Allele Identifier: PA645496569
Gene: HSD17B4 HGNC NCBI

Linked Data

ClinVar Variation Id: 228741
ClinVar RCV Id: RCV000222427 RCV000380697 RCV000731627 RCV000765793 RCV001083539 RCV004532757 RCV000344886
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001186220.1:p.Thr342Met
CA3382045
NM_001199291.3:c.1025C>T