Canonical Allele Identifier: PA2573223311
Gene: LAMB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1521297
ClinVar RCV Id: RCV002031209 RCV002294503
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002283.3:p.Pro1357Leu
CA2393879
NM_002292.4:c.4070C>T