Canonical Allele Identifier: PA645420951
Gene: LCT HGNC NCBI

Linked Data

ClinVar Variation Id: 331168
ClinVar RCV Id: RCV000349439 RCV000392923 RCV001511195 RCV001528850
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002290.2:p.Asn1639Ser
CA1887741
NM_002299.3:c.4916A>G