Canonical Allele Identifier: PA2825454513
Gene: LAMA2 HGNC NCBI

Linked Data

ClinVar Variation Id: 355303
ClinVar RCV Id: RCV000291071
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073291.2:p.Ile2874Ser
CA10622908
NM_001079823.2:c.8621T>G