Canonical Allele Identifier: PA2573062615
Gene: LAMA2 HGNC NCBI

Linked Data

ClinVar Variation Id: 477510
ClinVar RCV Id: RCV000544403
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000417.3:p.Thr2581Ser
CA365628438
NM_000426.4:c.7741A>T
CA365628442
NM_000426.4:c.7742C>G