Canonical Allele Identifier: PA312631
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_000402.3:p.Ser136Arg
CA312630
NM_000411.8:c.408C>G
CA409913102
NM_000411.8:c.408C>A
CA409913106
NM_000411.8:c.406A>C