Canonical Allele Identifier: PA658654763
Gene: HLCS HGNC NCBI

Linked Data

ClinVar Variation Id: 444575
ClinVar RCV Id: RCV000513287

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000402.3:p.Pro162Leu
CA10020674
NM_000411.8:c.485C>T