Canonical Allele Identifier: PA2826304127
Gene: HLCS HGNC NCBI

Linked Data

ClinVar Variation Id: 989621
ClinVar RCV Id: RCV001277488

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001229713.1:p.Tyr99Cys
CA10020706
NM_001242784.3:c.296A>G