Canonical Allele Identifier: PA2825167597
Gene: LAMA2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1481206
ClinVar RCV Id: RCV002000491
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000417.3:p.Glu1191Gly
CA365612631
NM_000426.4:c.3572A>G