Allele Registry

Canonical Allele Identifier: PA645420915

Gene: LCT HGNC NCBI

ClinVar RCV:

RCV000266315

RCV000316915

RCV001850777

ClinVar Variation:

331203

HGVS (amino-acid)	Matching Registered Transcripts
NP_002290.2:p.Gly466Trp	CA1888395 NM_002299.3:c.1396G>T