Canonical Allele Identifier: PA916035412
Gene: HLCS HGNC NCBI

Linked Data

ClinVar Variation Id: 379267
ClinVar RCV Id: RCV000429268 RCV002524831
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339443.1:p.Ser805Gly
CA10020274
NM_001352514.2:c.2413A>G