Canonical Allele Identifier: PA2580112567
Gene: LAMA2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1997327
ClinVar RCV Id: RCV002791712
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000417.3:p.Ala2572Val
CA365628339
NM_000426.4:c.7715C>T