Canonical Allele Identifier: PA2827652851
Gene: HLCS HGNC NCBI

Linked Data

ClinVar Variation Id: 1414474
ClinVar RCV Id: RCV001945303
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339445.1:p.Leu157Phe
CA10020678
NM_001352516.2:c.469C>T