Canonical Allele Identifier: PA2827651889
Gene: HLCS HGNC NCBI

Linked Data

ClinVar Variation Id: 843433
ClinVar RCV Id: RCV001046058

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339443.1:p.Pro194Leu
CA320395975
NM_001352514.2:c.581C>T