Canonical Allele Identifier: PA916035361
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_001339443.1:p.Ser283Arg
CA312630
NM_001352514.2:c.849C>G
CA409913102
NM_001352514.2:c.849C>A
CA409913106
NM_001352514.2:c.847A>C