Canonical Allele Identifier: PA2499260855
Gene: LAMB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1062779
ClinVar RCV Id: RCV001372535
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002283.3:p.Gly837Arg
CA352720826
NM_002292.4:c.2509G>A
CA352720828
NM_002292.4:c.2509G>C