Canonical Allele Identifier: PA2826304097
Gene: HLCS HGNC NCBI

Linked Data

ClinVar Variation Id: 2151394
ClinVar RCV Id: RCV003061318
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001229713.1:p.Leu49Phe
CA10020729
NM_001242784.3:c.145C>T