Canonical Allele Identifier: PA2827654060
Gene: HLCS HGNC NCBI

Linked Data

ClinVar Variation Id: 1929350
ClinVar RCV Id: RCV002618648

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339447.1:p.Gly301Arg
CA409912061
NM_001352518.2:c.901G>C