Canonical Allele Identifier: PA2573223348
Gene: LAMB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1491928
ClinVar RCV Id: RCV001989006 RCV002592658
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002283.3:p.Arg1490Gln
CA2393782
NM_002292.4:c.4469G>A