Canonical Allele Identifier: PA658675920
Gene: LAMB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 472484
ClinVar RCV Id: RCV000559112 RCV001145299 RCV001145300 RCV001764596 RCV003952833
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002283.3:p.Asp1373Gly
CA2393867
NM_002292.4:c.4118A>G