Canonical Allele Identifier: PA645379582
Gene: HLCS HGNC NCBI

Linked Data

ClinVar Variation Id: 379267
ClinVar RCV Id: RCV000429268 RCV002524831
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000402.3:p.Ser658Gly
CA10020274
NM_000411.8:c.1972A>G