Allele Registry

Canonical Allele Identifier: PA2825454672

Gene: LAMA2 HGNC NCBI

ClinVar RCV:

RCV000527451

RCV001151351

ClinVar Variation:

477523

HGVS (amino-acid)	Matching Registered Transcripts
NP_001073291.2:p.Val2960Leu	CA3994959 NM_001079823.2:c.8878G>T CA365636054 NM_001079823.2:c.8878G>C