Canonical Allele Identifier: PA2827653467
Gene: HLCS HGNC NCBI

Linked Data

ClinVar Variation Id: 570638
ClinVar RCV Id: RCV000691542 RCV001805808
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339446.1:p.Val218Phe
CA409912589
NM_001352517.1:c.652G>T