Canonical Allele Identifier: PA2573168401
Gene: LAMA2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1510526
ClinVar RCV Id: RCV002013937
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000417.3:p.Asp2880Tyr
CA365634903
NM_000426.4:c.8638G>T