Canonical Allele Identifier: PA2826304171
Gene: HLCS HGNC NCBI

Linked Data

ClinVar Variation Id: 444575
ClinVar RCV Id: RCV000513287

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001229713.1:p.Pro162Leu
CA10020674
NM_001242784.3:c.485C>T