Canonical Allele Identifier: PA1139733954
Gene: HLCS HGNC NCBI

Linked Data

ClinVar Variation Id: 965102
ClinVar RCV Id: RCV001239463
ClinVar Variation Id: 1199286
ClinVar RCV Id: RCV001563772

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339443.1:p.Gly472Arg
CA10020579
NM_001352514.2:c.1414G>A
CA409911904
NM_001352514.2:c.1414G>C