Canonical Allele Identifier: PA2827652400
Gene: HLCS HGNC NCBI

Linked Data

ClinVar Variation Id: 2156520
ClinVar RCV Id: RCV003084158

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339444.1:p.Leu285Ser
CA10020603
NM_001352515.2:c.854T>C