Canonical Allele Identifier: PA2573223314
Gene: LAMB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1399805
ClinVar RCV Id: RCV001893885 RCV003365528
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002283.3:p.His1366Arg
CA2393874
NM_002292.4:c.4097A>G