Canonical Allele Identifier: PA2827652926
Gene: HLCS HGNC NCBI

Linked Data

ClinVar Variation Id: 1907
ClinVar RCV Id: RCV000001984

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339445.1:p.Leu237Pro
CA278018
NM_001352516.2:c.710T>C