Canonical Allele Identifier: PA2825168655
Gene: LAMA2 HGNC NCBI

Linked Data

ClinVar Variation Id: 945403
ClinVar RCV Id: RCV001216035

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000417.3:p.Met2303Thr
CA3994392
NM_000426.4:c.6908T>C