Canonical Allele Identifier: PA2826304709
Gene: HLCS HGNC NCBI

Linked Data

ClinVar Variation Id: 203774
ClinVar RCV Id: RCV000185966
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001229714.1:p.Ser136Arg
CA312630
NM_001242785.2:c.408C>G
CA409913102
NM_001242785.2:c.408C>A
CA409913106
NM_001242785.2:c.406A>C