Canonical Allele Identifier: PA645420956
Gene: LCT HGNC NCBI

Linked Data

ClinVar Variation Id: 331162
ClinVar RCV Id: RCV000326698 RCV000360630 RCV000955964 RCV003972396
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002290.2:p.Pro1923Gln
CA1887547
NM_002299.3:c.5768C>A