Canonical Allele Identifier: PA2580276708
Gene: LAMB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2032530
ClinVar RCV Id: RCV002884972
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002283.3:p.Asp1496Glu
CA2393777
NM_002292.4:c.4488C>A
CA352692346
NM_002292.4:c.4488C>G