Canonical Allele Identifier: PA105380
Gene: HSD17B4 HGNC NCBI

Linked Data

ClinVar Variation Id: 7656
ClinVar RCV Id: RCV000008095 RCV000385297 RCV000477799 RCV000684773 RCV001002204
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000405.1:p.Asn457Tyr
CA118961
NM_000414.4:c.1369A>T