Canonical Allele Identifier: PA2826304897
Gene: HLCS HGNC NCBI
ClinVar RCV:
RCV002630302
ClinVar Variation:
1919466
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001229714.1:p.Ala391Thr
CA409910981
NM_001242785.2:c.1171G>A