Canonical Allele Identifier: PA2825167032
Gene: LAMA2 HGNC NCBI

Linked Data

ClinVar Variation Id: 551956
ClinVar RCV Id: RCV000667133 RCV001861755 RCV002507156
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000417.3:p.Val598del
CA570053408
NM_000426.4:c.1793_1795del