Allele Registry

Canonical Allele Identifier: PA104101

Gene: LCT HGNC NCBI

ClinVar RCV:

RCV000049801

ClinVar Variation:

56388

HGVS (amino-acid)	Matching Registered Transcripts
NP_002290.2:p.Gly1363Ser	CA144313 NM_002299.3:c.4087G>A