ClinGen Allele Registry
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Canonical Allele Identifier:
PA915966901
Gene: LAMA2
HGNC
NCBI
Linked Data
ClinVar RCV:
RCV000518091
RCV000560647
RCV001333431
RCV001507676
RCV002525050
ClinVar Variation:
447680
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001073291.2:p.Lys467Arg
CA3992597
NM_001079823.2:c.1400A>G