Canonical Allele Identifier: PA2827654028
Gene: HLCS HGNC NCBI

Linked Data

ClinVar Variation Id: 809289
ClinVar RCV Id: RCV000997829
ClinVar Variation Id: 1039991
ClinVar RCV Id: RCV001343560
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339447.1:p.His264Gln
CA409912292
NM_001352518.2:c.792C>A
CA409912293
NM_001352518.2:c.792C>G