Canonical Allele Identifier: PA123689
Gene: MATR3 HGNC NCBI

Linked Data

ClinVar Variation Id: 14002

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_061322.2:p.Ser85Cys
CA123688
NM_018834.6:c.254C>G