Canonical Allele Identifier: PA2825167639
Gene: LAMA2 HGNC NCBI

Linked Data

ClinVar Variation Id: 965595
ClinVar RCV Id: RCV001240086

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000417.3:p.Pro1232Thr
CA3993332
NM_000426.4:c.3694C>A