Canonical Allele Identifier: PA2826304785
Gene: HLCS HGNC NCBI

Linked Data

ClinVar Variation Id: 1366602
ClinVar RCV Id: RCV001962105
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001229714.1:p.Glu227Asp
CA10020631
NM_001242785.2:c.681A>C
CA409912530
NM_001242785.2:c.681A>T