Canonical Allele Identifier: PA1139716646
Gene: LAMB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 847455
ClinVar RCV Id: RCV001051003
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002283.3:p.Glu1506Lys
CA352691954
NM_002292.4:c.4516G>A