Canonical Allele Identifier: PA2573223748
Gene: LCT HGNC NCBI

Linked Data

ClinVar Variation Id: 1393156
ClinVar RCV Id: RCV001898173 RCV002553638
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002290.2:p.Thr1802Ala
CA1887617
NM_002299.3:c.5404A>G