Canonical Allele Identifier: PA105692
Gene: HSD17B3 HGNC NCBI

Linked Data

ClinVar Variation Id: 2440772
ClinVar RCV Id: RCV003146073 RCV003561189
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000188.1:p.Glu215Asp
CA5140317
NM_000197.2:c.645A>T
CA374123528
NM_000197.2:c.645A>C