Allele Registry

Canonical Allele Identifier: PA2825166486

Gene: LAMA2 HGNC NCBI

ClinVar Allele:

368311

ClinVar RCV:

RCV000514861

RCV001083278

RCV001156178

RCV004022339

RCV004532993

ClinVar Variation:

381265

HGVS (amino-acid)	Matching Registered Transcripts
NP_000417.3:p.Pro25Leu	CA3992202 NM_000426.4:c.74C>T