Canonical Allele Identifier: PA2573223584
Gene: LCT HGNC NCBI

Linked Data

ClinVar Variation Id: 1525159

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002290.2:p.Gly554Ser
CA56623342
NM_002299.3:c.1660G>A