Allele Registry

Canonical Allele Identifier: PA2573062650

Gene: LAMA2 HGNC NCBI

ClinVar Allele:

455276

ClinVar RCV:

RCV000527451

RCV001151351

ClinVar Variation:

477523

HGVS (amino-acid)	Matching Registered Transcripts
NP_000417.3:p.Val2964Leu	CA3994959 NM_000426.4:c.8890G>T CA365636054 NM_000426.4:c.8890G>C