Canonical Allele Identifier: PA104934
Gene: MATN3 HGNC NCBI

Linked Data

ClinVar Variation Id: 7546
ClinVar RCV Id: RCV000007982
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002372.1:p.Ala128Pro
CA254205
NM_002381.5:c.382G>C