Allele Registry

Canonical Allele Identifier: PA2826304971

Gene: HLCS HGNC NCBI

ClinVar RCV:

RCV002039362

ClinVar Variation:

1349920

HGVS (amino-acid)	Matching Registered Transcripts
NP_001229714.1:p.Met493Ile	CA409921907 NM_001242785.2:c.1479G>T CA409921909 NM_001242785.2:c.1479G>C CA409921912 NM_001242785.2:c.1479G>A