Canonical Allele Identifier: PA2825660247
Gene: LAMA3 HGNC NCBI

Linked Data

ClinVar Variation Id: 1315022

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121190.2:p.Asn917Ser
CA8916736
NM_001127718.2:c.2750A>G