Canonical Allele Identifier: PA105148
Gene: HLCS HGNC NCBI
ClinVar RCV:
RCV003468353
ClinVar Variation:
2676026
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000402.3:p.Asn511Lys
CA409921204
NM_000411.8:c.1533T>A
CA409921207
NM_000411.8:c.1533T>G