Canonical Allele Identifier: PA2573223318
Gene: LAMB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1429698
ClinVar RCV Id: RCV001950149
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002283.3:p.Arg1367Pro
CA2393872
NM_002292.4:c.4100G>C