Canonical Allele Identifier: PA2826304257
Gene: HLCS HGNC NCBI

Linked Data

ClinVar Variation Id: 809289
ClinVar RCV Id: RCV000997829
ClinVar Variation Id: 1039991
ClinVar RCV Id: RCV001343560

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001229713.1:p.His264Gln
CA409912292
NM_001242784.3:c.792C>A
CA409912293
NM_001242784.3:c.792C>G