ClinGen Allele Registry
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Canonical Allele Identifier:
PA2825168032
Gene: LAMA2
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000524771
RCV000712188
RCV001153956
RCV002526746
ClinVar Variation:
477478
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000417.3:p.Glu1637Lys
CA3993714
NM_000426.4:c.4909G>A