Canonical Allele Identifier: PA2826304162
Gene: HLCS HGNC NCBI

Linked Data

ClinVar Variation Id: 1389284
ClinVar RCV Id: RCV001887105 RCV004039104
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001229713.1:p.Asn156Ile
CA320395694
NM_001242784.3:c.467A>T