Canonical Allele Identifier: PA2580148500
Gene: LAMA2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2144139
ClinVar RCV Id: RCV003053258

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073291.2:p.Phe1233Leu
CA365613056
NM_001079823.2:c.3697T>C
CA365613061
NM_001079823.2:c.3699T>A
CA365613062
NM_001079823.2:c.3699T>G