Canonical Allele Identifier: PA2825167631
Gene: LAMA2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2008956
ClinVar RCV Id: RCV002829026

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000417.3:p.Asp1227Val
CA365613002
NM_000426.4:c.3680A>T