Canonical Allele Identifier: PA2827653951
Gene: HLCS HGNC NCBI

Linked Data

ClinVar Variation Id: 2725471
ClinVar RCV Id: RCV003499619
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339447.1:p.Asp171Asn
CA320395621
NM_001352518.2:c.511G>A