Canonical Allele Identifier: PA2573223739
Gene: LCT HGNC NCBI

Linked Data

ClinVar Variation Id: 1519067
ClinVar RCV Id: RCV002024330

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002290.2:p.Gln1622His
CA1887767
NM_002299.3:c.4866G>T
CA348592280
NM_002299.3:c.4866G>C