Canonical Allele Identifier: PA123689
Gene: MATR3 HGNC NCBI

Linked Data

ClinVar Variation Id: 14002
ClinVar RCV Id: RCV000015039 RCV000517083
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Amino-acid Alleles

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