Allele Registry

Canonical Allele Identifier: PA915967470

Gene: LAMA2 HGNC NCBI

ClinVar Allele:

98876

ClinVar RCV:

RCV000078780

RCV000872576

RCV001152796

RCV001719818

ClinVar Variation:

92969

HGVS (amino-acid)	Matching Registered Transcripts
NP_001073291.2:p.Ser1878Phe	CA146142 NM_001079823.2:c.5633C>T