Canonical Allele Identifier: PA658831232
Gene: HLCS HGNC NCBI

Linked Data

ClinVar Variation Id: 1908

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001229714.1:p.Asp571Asn
CA278019
NM_001242785.2:c.1711G>A