Canonical Allele Identifier: PA2827652872
Gene: HLCS HGNC NCBI

Linked Data

ClinVar Variation Id: 1430063
ClinVar RCV Id: RCV001931311

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339445.1:p.Gly177Ser
CA10020664
NM_001352516.2:c.529G>A