Allele Registry

Canonical Allele Identifier: PA2825168261

Gene: LAMA2 HGNC NCBI

ClinVar Allele:

98876

ClinVar RCV:

RCV000078780

RCV000872576

RCV001152796

RCV001719818

ClinVar Variation:

92969

HGVS (amino-acid)	Matching Registered Transcripts
NP_000417.3:p.Ser1878Phe	CA146142 NM_000426.4:c.5633C>T