ClinGen Allele Registry
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Canonical Allele Identifier:
PA118362
Gene: LCT
HGNC
NCBI
Linked Data
JSON-LD
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