Canonical Allele Identifier: PA2825167628
Gene: LAMA2 HGNC NCBI

Linked Data

ClinVar Variation Id: 355266

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000417.3:p.Asp1222Glu
CA3993326
NM_000426.4:c.3666C>A
CA365612951
NM_000426.4:c.3666C>G