Canonical Allele Identifier: PA105078
Gene: MATN3 HGNC NCBI

Linked Data

ClinVar Variation Id: 7540
ClinVar RCV Id: RCV000007976 RCV002054422
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002372.1:p.Val194Asp
CA254202
NM_002381.5:c.581T>A