Canonical Allele Identifier: PA2827653237
Gene: HLCS HGNC NCBI

Linked Data

ClinVar Variation Id: 379267

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339445.1:p.Ser658Gly
CA10020274
NM_001352516.2:c.1972A>G