Allele Registry

Canonical Allele Identifier: PA104084

Gene: LCT HGNC NCBI

ClinVar RCV:

RCV000006966

ClinVar Variation:

6588

HGVS (amino-acid)	Matching Registered Transcripts
NP_002290.2:p.Gln268His	CA118363 NM_002299.3:c.804G>C CA348608518 NM_002299.3:c.804G>T