Canonical Allele Identifier: PA103690
Gene: HMGCS2 HGNC NCBI

Linked Data

ClinVar Variation Id: 9259
ClinVar RCV Id: RCV000009841 RCV000498667
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005509.1:p.Gly212Arg
CA120256
NM_005518.4:c.634G>A
CA341862957
NM_005518.4:c.634G>C