Canonical Allele Identifier: PA2825454810
Gene: LAMA2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1373865
ClinVar RCV Id: RCV001877534

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073291.2:p.Lys3070Asn
CA365637203
NM_001079823.2:c.9210G>C
CA365637204
NM_001079823.2:c.9210G>T