Canonical Allele Identifier: PA120261
Gene: HMGCS2 HGNC NCBI

Linked Data

ClinVar Variation Id: 9260
ClinVar RCV Id: RCV000009842
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159579.1:p.Arg458His
CA120258
NM_001166107.1:c.1373G>A