ClinGen Allele Registry
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Canonical Allele Identifier:
PA915988589
Gene: LAMB2
HGNC
NCBI
Linked Data
ClinVar Variation Id:
644453
ClinVar RCV Id:
RCV000798371
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_002283.3:p.Ser1472Thr
CA352693150
NM_002292.4:c.4415G>C