Canonical Allele Identifier: PA2825167871
Gene: LAMA2 HGNC NCBI

Linked Data

ClinVar Variation Id: 557224
ClinVar RCV Id: RCV000673335 RCV002066980
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000417.3:p.Arg1493Cys
CA3993566
NM_000426.4:c.4477C>T