Canonical Allele Identifier: PA2573223312
Gene: LAMB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1511759
ClinVar RCV Id: RCV002016900
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002283.3:p.Ser1359Gly
CA352696744
NM_002292.4:c.4075A>G