Canonical Allele Identifier: PA915967279
Gene: LAMA2 HGNC NCBI

Linked Data

ClinVar Variation Id: 497342
ClinVar RCV Id: RCV000595680 RCV002530976
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073291.2:p.His1229Tyr
CA146914097
NM_001079823.2:c.3685C>T