Canonical Allele Identifier: PA2825166923
Gene: LAMA2 HGNC NCBI

Linked Data

ClinVar Variation Id: 940384
ClinVar RCV Id: RCV001209959
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000417.3:p.Phe505Leu
CA3992641
NM_000426.4:c.1513T>C
CA365607861
NM_000426.4:c.1515C>A
CA365607862
NM_000426.4:c.1515C>G