Canonical Allele Identifier: PA2573177234
Gene: LAMA2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1501770
ClinVar RCV Id: RCV002010810

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073291.2:p.Gly1209Asp
CA365612806
NM_001079823.2:c.3626G>A