Canonical Allele Identifier: PA2829304608
Gene: MATR3 HGNC NCBI
ClinVar RCV:
RCV003515572
ClinVar Variation:
2707802
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001387385.1:p.Trp178Arg
CA361487472
NM_001400456.1:c.532T>A
CA361487473
NM_001400456.1:c.532T>C