Allele Registry

Canonical Allele Identifier: PA915999709

Gene: LAMA1 HGNC NCBI

ClinVar RCV:

RCV000968363

ClinVar Variation:

786327

HGVS (amino-acid)	Matching Registered Transcripts
NP_005550.2:p.Thr2611Pro	CA8880768 NM_005559.4:c.7831A>C