Canonical Allele Identifier: PA2825167852
Gene: LAMA2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1714836
ClinVar RCV Id: RCV002304416

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000417.3:p.Pro1472Ser
CA365615508
NM_000426.4:c.4414C>T