Canonical Allele Identifier: PA2580276839
Gene: LCT HGNC NCBI

Linked Data

ClinVar Variation Id: 1970102
ClinVar RCV Id: RCV002730369

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002290.2:p.Leu217Phe
CA348608857
NM_002299.3:c.649C>T