Canonical Allele Identifier: PA2827652782
Gene: HLCS HGNC NCBI

Linked Data

ClinVar Variation Id: 843433
ClinVar RCV Id: RCV001046058
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339445.1:p.Pro47Leu
CA320395975
NM_001352516.2:c.140C>T