ClinGen Allele Registry
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Canonical Allele Identifier:
PA645485405
Gene: LAMB2
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000247257
RCV000307336
RCV000371274
RCV000556669
RCV000712177
RCV002294127
ClinVar Variation:
258605
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_002283.3:p.Gly914Arg
CA2394217
NM_002292.4:c.2740G>A
CA2394218
NM_002292.4:c.2740G>C