Canonical Allele Identifier: PA2580276844
Gene: LCT HGNC NCBI

Linked Data

ClinVar Variation Id: 2306379
ClinVar RCV Id: RCV002869841
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002290.2:p.Leu230Pro
CA348608780
NM_002299.3:c.689T>C