Canonical Allele Identifier: PA110473
Gene: MATR3 HGNC NCBI

Linked Data

ClinVar Variation Id: 14002

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001181883.1:p.Ser85Cys
CA123688
NM_001194954.2:c.254C>G