Canonical Allele Identifier: PA1139716636
Gene: LAMB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 930193
ClinVar RCV Id: RCV001195701 RCV001859179
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002283.3:p.Arg1436His
CA2393813
NM_002292.4:c.4307G>A