Canonical Allele Identifier: PA2580276965
Gene: LCT HGNC NCBI

Linked Data

ClinVar Variation Id: 1940641
ClinVar RCV Id: RCV002658509
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002290.2:p.Arg1659Trp
CA1887728
NM_002299.3:c.4975C>T