Canonical Allele Identifier: PA2825659407
Gene: LAMA3 HGNC NCBI

Linked Data

ClinVar Variation Id: 1315022

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121189.2:p.Asn2526Ser
CA8916736
NM_001127717.2:c.7577A>G