Canonical Allele Identifier: PA2827653411
Gene: HLCS HGNC NCBI

Linked Data

ClinVar Variation Id: 1944989
ClinVar RCV Id: RCV002663293

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339446.1:p.Asn156Lys
CA409912971
NM_001352517.1:c.468C>G
CA409912972
NM_001352517.1:c.468C>A