Canonical Allele Identifier: PA2499260881
Gene: LAMB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1004294
ClinVar RCV Id: RCV001300978
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002283.3:p.Ala1487Ser
CA74476336
NM_002292.4:c.4459G>T