Canonical Allele Identifier: PA2580208599
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_001339443.1:p.Gly472Trp
CA10020578
NM_001352514.2:c.1414G>T