Canonical Allele Identifier: PA2827653546
Gene: HLCS HGNC NCBI

Linked Data

ClinVar Variation Id: 418250
ClinVar RCV Id: RCV000478103 RCV001405509 RCV002526512
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339446.1:p.Val317Leu
CA10020583
NM_001352517.1:c.949G>T
CA409911951
NM_001352517.1:c.949G>C