Canonical Allele Identifier: PA2580276870
Gene: LCT HGNC NCBI

Linked Data

ClinVar Variation Id: 1918552
ClinVar RCV Id: RCV002602025
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002290.2:p.Asp431Asn
CA1888411
NM_002299.3:c.1291G>A