Canonical Allele Identifier: PA2499260875
Gene: LAMB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1029435
ClinVar RCV Id: RCV001330712 RCV004035702
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002283.3:p.Arg1367Trp
CA2393873
NM_002292.4:c.4099C>T