Canonical Allele Identifier: PA2825168697
Gene: LAMA2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1014560
ClinVar RCV Id: RCV001313311
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000417.3:p.Ser2352Thr
CA3994426
NM_000426.4:c.7055G>C