Canonical Allele Identifier: PA2826607109
Gene: LIAS HGNC NCBI

Linked Data

ClinVar Variation Id: 839857
ClinVar RCV Id: RCV001041713
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001265519.1:p.Cys22Trp
CA95724854
NM_001278590.2:c.66C>G