Canonical Allele Identifier: PA2573062612
Gene: LAMA2 HGNC NCBI

Linked Data

ClinVar Variation Id: 14294

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000417.3:p.Leu2564Pro
CA257207
NM_000426.4:c.7691T>C