Canonical Allele Identifier: PA2499261090
Gene: MATN3 HGNC NCBI

Linked Data

ClinVar Variation Id: 1062861
ClinVar RCV Id: RCV001372625

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002372.1:p.Leu146Pro
CA345951090
NM_002381.5:c.437T>C