Canonical Allele Identifier: PA2827654269
Gene: HLCS HGNC NCBI

Linked Data

ClinVar Variation Id: 529441
ClinVar RCV Id: RCV000634878
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339447.1:p.Val604Met
CA409919494
NM_001352518.2:c.1810G>A