Canonical Allele Identifier: PA2580265653
Gene: MATN3 HGNC NCBI

Linked Data

ClinVar Variation Id: 2089476
ClinVar RCV Id: RCV003005571
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002372.1:p.Ile193Thr
CA1543947
NM_002381.5:c.578T>C