Canonical Allele Identifier: PA2826304782
Gene: HLCS HGNC NCBI

Linked Data

ClinVar Variation Id: 2615307
ClinVar RCV Id: RCV003365264
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001229714.1:p.Arg222Gly
CA409912566
NM_001242785.2:c.664A>G