Canonical Allele Identifier: PA2825167612
Gene: LAMA2 HGNC NCBI

Linked Data

ClinVar Variation Id: 129438

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000417.3:p.Thr1205Ala
CA153439
NM_000426.4:c.3613A>G