Canonical Allele Identifier: PA2825168717
Gene: LAMA2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1394950
ClinVar RCV Id: RCV001898665

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000417.3:p.Phe2371Ser
CA3994443
NM_000426.4:c.7112T>C