ClinGen Allele Registry
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Canonical Allele Identifier:
PA915967298
Gene: LAMA2
HGNC
NCBI
Linked Data
ClinVar RCV:
RCV000541809
RCV000664838
RCV001158142
RCV001508559
RCV002483507
ClinVar Variation:
477467
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001073291.2:p.His1337Arg
CA3993409
NM_001079823.2:c.4010A>G