Canonical Allele Identifier: PA2573223579
Gene: LCT HGNC NCBI

Linked Data

ClinVar Variation Id: 1402901
ClinVar RCV Id: RCV001908772 RCV003167076
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002290.2:p.Ala523Val
CA1888376
NM_002299.3:c.1568C>T