Canonical Allele Identifier: PA2573062559
Gene: LAMA2 HGNC NCBI

Linked Data

ClinVar Variation Id: 576235
ClinVar RCV Id: RCV000698683
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000417.3:p.Arg2578Gly
CA365628402
NM_000426.4:c.7732C>G