Canonical Allele Identifier: PA118362
Gene: LCT HGNC NCBI

Linked Data


Amino-acid Alleles

HGVS (amino-acid) Transcript change
NP_002290.2:p.Tyr1390Ter
NM_002299.3:c.4170T>A

NM_002299.3:c.4170T>G