Canonical Allele Identifier: PA2825167057
Gene: LAMA2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1503543
ClinVar RCV Id: RCV002045454
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000417.3:p.Arg619Ser
CA365609621
NM_000426.4:c.1855C>A