Canonical Allele Identifier: PA658660389
Gene: HMGCS2 HGNC NCBI

Linked Data

ClinVar Variation Id: 449457
ClinVar RCV Id: RCV000520978 RCV002525119
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005509.1:p.Gly388Arg
CA1037663
NM_005518.4:c.1162G>A
CA341858723
NM_005518.4:c.1162G>C