Allele Registry

Canonical Allele Identifier: PA2573062617

Gene: LAMA2 HGNC NCBI

ClinVar RCV:

RCV000031900

RCV001352555

RCV003144116

ClinVar Variation:

38341

HGVS (amino-acid)	Matching Registered Transcripts
NP_000417.3:p.His2627Gln	CA342967 NM_000426.4:c.7881T>G CA365629504 NM_000426.4:c.7881T>A