Canonical Allele Identifier: PA2573223337
Gene: LAMB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1448804
ClinVar RCV Id: RCV002012240
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002283.3:p.Ser1441Arg
CA352694168
NM_002292.4:c.4323C>G
CA352694178
NM_002292.4:c.4323C>A
CA352694216
NM_002292.4:c.4321A>C