Canonical Allele Identifier: PA2827653538
Gene: HLCS HGNC NCBI

Linked Data

ClinVar Variation Id: 418249

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339446.1:p.Arg302Ser
CA10020590
NM_001352517.1:c.906G>C
CA409912051
NM_001352517.1:c.906G>T