ClinGen Allele Registry
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Canonical Allele Identifier:
PA2825167181
Gene: LAMA2
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000533655
RCV000657928
RCV001156365
ClinVar Variation:
477452
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000417.3:p.Ala763Val
CA3992880
NM_000426.4:c.2288C>T