Canonical Allele Identifier: PA2827654074
Gene: HLCS HGNC NCBI

Linked Data

ClinVar Variation Id: 2146762
ClinVar RCV Id: RCV003076841
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339447.1:p.Gly325Trp
CA10020578
NM_001352518.2:c.973G>T