Canonical Allele Identifier: PA312639
Gene: HMGCS2 HGNC NCBI

Linked Data

ClinVar Variation Id: 203778
ClinVar RCV Id: RCV000185971 RCV000647361
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159579.1:p.Pro25Ala
CA312636
NM_001166107.1:c.73C>G