Allele Registry

Canonical Allele Identifier: PA2825166966

Gene: LAMA2 HGNC NCBI

ClinVar Allele:

493421

ClinVar RCV:

RCV000594834

RCV001064111

ClinVar Variation:

501997

HGVS (amino-acid)	Matching Registered Transcripts
NP_000417.3:p.Pro549Ser	CA3992684 NM_000426.4:c.1645C>T