Canonical Allele Identifier: PA915990103
Gene: MATN3 HGNC NCBI

Linked Data

ClinVar Variation Id: 801652

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002372.1:p.Val220Ala
CA1543930
NM_002381.5:c.659T>C