Canonical Allele Identifier: PA658802646
Gene: HLCS HGNC NCBI

Linked Data

ClinVar Variation Id: 529441
ClinVar RCV Id: RCV000634878

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000402.3:p.Val604Met
CA409919494
NM_000411.8:c.1810G>A