Allele Registry

Canonical Allele Identifier: PA104957

Gene: MATN3 HGNC NCBI

ClinVar RCV:

RCV000007979

RCV002054424

ClinVar Variation:

7543

HGVS (amino-acid)	Matching Registered Transcripts
NP_002372.1:p.Ala219Asp	CA254203 NM_002381.5:c.656C>A