Canonical Allele Identifier: PA2573223309
Gene: LAMB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1360685
ClinVar RCV Id: RCV001865014
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002283.3:p.Ser1356Asn
CA352696851
NM_002292.4:c.4067G>A