Canonical Allele Identifier: PA2826304744
Gene: HLCS HGNC NCBI

Linked Data

ClinVar Variation Id: 1430063
ClinVar RCV Id: RCV001931311
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001229714.1:p.Gly177Ser
CA10020664
NM_001242785.2:c.529G>A