Canonical Allele Identifier: PA118877
Gene: MATN3 HGNC NCBI

Linked Data

ClinVar Variation Id: 7542
ClinVar RCV Id: RCV000007978 RCV000318887 RCV000733135 RCV001522562 RCV002276539 RCV003904818
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002372.1:p.Thr303Met
CA118876
NM_002381.5:c.908C>T