Canonical Allele Identifier: PA2825164041
Gene: HLCS HGNC NCBI

Linked Data

ClinVar Variation Id: 2495243
ClinVar RCV Id: RCV003213421

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000402.3:p.Tyr99Phe
CA409913360
NM_000411.8:c.296A>T