Canonical Allele Identifier: PA2580148540
Gene: LAMA2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2061577
ClinVar RCV Id: RCV002942837
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073291.2:p.Arg1493His
CA3993567
NM_001079823.2:c.4478G>A