Canonical Allele Identifier: PA2825168711
Gene: LAMA2 HGNC NCBI

Linked Data

ClinVar Variation Id: 435714
ClinVar RCV Id: RCV000500474 RCV000557131 RCV000764632 RCV001509285 RCV004541559
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000417.3:p.Thr2363Ile
CA3994438
NM_000426.4:c.7088C>T