ClinGen Allele Registry
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Canonical Allele Identifier:
PA2825168441
Gene: LAMA2
HGNC
NCBI
Linked Data
ClinVar RCV:
RCV000509339
RCV000527643
RCV001821424
RCV003133294
ClinVar Variation:
440937
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000417.3:p.Ala2077Thr
CA3994141
NM_000426.4:c.6229G>A