Canonical Allele Identifier: PA2826818689
Gene: HSD17B4 HGNC NCBI
ClinVar RCV:
RCV001882203
ClinVar Variation:
1392532
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001278956.1:p.Asp20Val
CA125857517
NM_001292027.2:c.59A>T