Canonical Allele Identifier: PA2573222946
Gene: LAMB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1374660
ClinVar RCV Id: RCV001879270 RCV003164230
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002283.3:p.Lys313Arg
CA2394747
NM_002292.4:c.938A>G