Canonical Allele Identifier: PA2825168656
Gene: LAMA2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1444372
ClinVar RCV Id: RCV001982378

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000417.3:p.Met2303Ile
CA365619161
NM_000426.4:c.6909G>A
CA365619162
NM_000426.4:c.6909G>T
CA365619163
NM_000426.4:c.6909G>C