Canonical Allele Identifier: PA2580148678
Gene: LAMA2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1980729
ClinVar RCV Id: RCV002780323

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073291.2:p.Val2400Ile
CA146892066
NM_001079823.2:c.7198G>A