Canonical Allele Identifier: PA2826640854
Gene: MATR3 HGNC NCBI

Linked Data

ClinVar Variation Id: 351136
ClinVar RCV Id: RCV000326793

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269207.1:p.Ser410Pro
CA3433397
NM_001282278.2:c.1228T>C