Canonical Allele Identifier: PA2827652961
Gene: HLCS HGNC NCBI

Linked Data

ClinVar Variation Id: 2156520
ClinVar RCV Id: RCV003084158
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339445.1:p.Leu285Ser
CA10020603
NM_001352516.2:c.854T>C