Canonical Allele Identifier: PA2573168325
Gene: LAMA2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1401419
ClinVar RCV Id: RCV001911800
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000417.3:p.Leu2565Ser
CA365628251
NM_000426.4:c.7694T>C