Canonical Allele Identifier: PA2827653941
Gene: HLCS HGNC NCBI

Linked Data

ClinVar Variation Id: 444575
ClinVar RCV Id: RCV000513287
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339447.1:p.Pro162Leu
CA10020674
NM_001352518.2:c.485C>T