Canonical Allele Identifier: PA2827652253
Gene: HLCS HGNC NCBI

Linked Data

ClinVar Variation Id: 2495243
ClinVar RCV Id: RCV003213421

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339444.1:p.Tyr99Phe
CA409913360
NM_001352515.2:c.296A>T