Canonical Allele Identifier: PA2741892186
Gene: LCT HGNC NCBI

Linked Data

ClinVar Variation Id: 2540753
ClinVar RCV Id: RCV003294901

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002290.2:p.Ala1588Ser
CA348592978
NM_002299.3:c.4762G>T