Canonical Allele Identifier: PA2825164707
Gene: HSD17B4 HGNC NCBI

Linked Data

ClinVar Variation Id: 2944570
ClinVar RCV Id: RCV003808272
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000405.1:p.Asn98Lys
CA360864889
NM_000414.4:c.294C>A
CA360864890
NM_000414.4:c.294C>G