Canonical Allele Identifier: PA2580276871
Gene: LCT HGNC NCBI

Linked Data

ClinVar Variation Id: 2303570
ClinVar RCV Id: RCV002891369
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002290.2:p.Ala441Thr
CA1888406
NM_002299.3:c.1321G>A