Canonical Allele Identifier: PA2573061863
Gene: LAMA3 HGNC NCBI

Linked Data

ClinVar Variation Id: 1315022

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000218.3:p.Asn973Ser
CA8916736
NM_000227.6:c.2918A>G