Canonical Allele Identifier: PA2828525509
Gene: HSD17B4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1685886
ClinVar RCV Id: RCV002250053
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361429.1:p.Leu31Phe
CA360866267
NM_001374500.1:c.91C>T