Canonical Allele Identifier: PA658826763
Gene: HSD17B4 HGNC NCBI

Linked Data

ClinVar Variation Id: 556974
ClinVar RCV Id: RCV000673049 RCV001861817 RCV002532141
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000405.1:p.Ala100Ser
CA360864901
NM_000414.4:c.298G>T