Canonical Allele Identifier: PA2827653956
Gene: HLCS HGNC NCBI

Linked Data

ClinVar Variation Id: 1430063
ClinVar RCV Id: RCV001931311

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339447.1:p.Gly177Ser
CA10020664
NM_001352518.2:c.529G>A