Canonical Allele Identifier: PA658832907
Gene: HSD17B4 HGNC NCBI

Linked Data

ClinVar Variation Id: 554819
ClinVar RCV Id: RCV000670516 RCV001448029
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001186220.1:p.Val38Ile
CA3381663
NM_001199291.3:c.112G>A