Canonical Allele Identifier: PA2826304979
Gene: HLCS HGNC NCBI

Linked Data

ClinVar Variation Id: 339961
ClinVar RCV Id: RCV000302979
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001229714.1:p.Arg501Gln
CA10644688
NM_001242785.2:c.1502G>A