Canonical Allele Identifier: PA2828525520
Gene: HSD17B4 HGNC NCBI

Linked Data

ClinVar Variation Id: 2937767
ClinVar RCV Id: RCV003794397
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361429.1:p.Ala49Glu
CA360866385
NM_001374500.1:c.146C>A