Canonical Allele Identifier: PA2573223738
Gene: LCT HGNC NCBI

Linked Data

ClinVar Variation Id: 1486234
ClinVar RCV Id: RCV002003445

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002290.2:p.Tyr1620His
CA348592310
NM_002299.3:c.4858T>C