Canonical Allele Identifier: PA104967
Gene: MATN3 HGNC NCBI

Linked Data

ClinVar Variation Id: 7541

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002372.1:p.Arg121Trp
CA340687
NM_002381.5:c.361C>T