ClinGen Allele Registry
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Canonical Allele Identifier:
PA915966791
Gene: LAMA2
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000517812
RCV001591167
RCV001851444
ClinVar Variation:
447686
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001073291.2:p.Tyr163Phe
CA3992348
NM_001079823.2:c.488A>T