Canonical Allele Identifier: PA2826818793
Gene: HSD17B4 HGNC NCBI

Linked Data

ClinVar Variation Id: 3107138
ClinVar RCV Id: RCV004404492
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001278956.1:p.Ile163Met
CA360866331
NM_001292027.2:c.489T>G