Canonical Allele Identifier: PA2573223750
Gene: LCT HGNC NCBI

Linked Data

ClinVar Variation Id: 1471626
ClinVar RCV Id: RCV001975687
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002290.2:p.Ser1816Arg
CA348586454
NM_002299.3:c.5448T>G
CA348586455
NM_002299.3:c.5448T>A
CA348586460
NM_002299.3:c.5446A>C