Canonical Allele Identifier: PA2580276555
Gene: LAMB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2260617
ClinVar RCV Id: RCV002788471
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002283.3:p.Pro335Leu
CA2394730
NM_002292.4:c.1004C>T