Canonical Allele Identifier: PA2825166945
Gene: LAMA2 HGNC NCBI

Linked Data

ClinVar Variation Id: 938363
ClinVar RCV Id: RCV001207564 RCV003130182
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000417.3:p.Ser530Cys
CA3992654
NM_000426.4:c.1589C>G