Canonical Allele Identifier: PA645485513
Gene: LAMB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 345973
ClinVar RCV Id: RCV000272339 RCV000321246 RCV000551379 RCV001753812 RCV003401366 RCV002520156
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002283.3:p.Ala1680Val
CA2393624
NM_002292.4:c.5039C>T