Canonical Allele Identifier: PA2826304126
Gene: HLCS HGNC NCBI

Linked Data

ClinVar Variation Id: 2495243
ClinVar RCV Id: RCV003213421

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001229713.1:p.Tyr99Phe
CA409913360
NM_001242784.3:c.296A>T