Canonical Allele Identifier: PA120269
Gene: HMGCS2 HGNC NCBI

Linked Data

ClinVar Variation Id: 9262
ClinVar RCV Id: RCV000009844
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159579.1:p.Tyr167Cys
CA120266
NM_001166107.1:c.500A>G