Canonical Allele Identifier: PA2826194720
Gene: MATR3 HGNC NCBI

Linked Data

ClinVar Variation Id: 2707802
ClinVar RCV Id: RCV003515572
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001181884.1:p.Trp178Arg
CA361487472
NM_001194955.2:c.532T>A
CA361487473
NM_001194955.2:c.532T>C