Canonical Allele Identifier: PA2827654322
Gene: HLCS HGNC NCBI

Linked Data

ClinVar Variation Id: 379267

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339447.1:p.Ser658Gly
CA10020274
NM_001352518.2:c.1972A>G