Canonical Allele Identifier: PA2825167066
Gene: LAMA2 HGNC NCBI

Linked Data

ClinVar Variation Id: 194173
ClinVar RCV Id: RCV000174479

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000417.3:p.Glu628Lys
CA240014
NM_000426.4:c.1882G>A