Canonical Allele Identifier: PA2827653668
Gene: HLCS HGNC NCBI

Linked Data

ClinVar Variation Id: 2044654
ClinVar RCV Id: RCV002900317
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339446.1:p.Ala499Val
CA10020421
NM_001352517.1:c.1496C>T