Canonical Allele Identifier: PA151203
Gene: MATR3 HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_954659.1:p.Phe115Cys
CA151202
NM_199189.3:c.344T>G