Allele Registry

Canonical Allele Identifier: PA105387

Gene: MMP13 HGNC NCBI

ClinVar RCV:

RCV000010050

RCV002512957

ClinVar Variation:

9443

HGVS (amino-acid)	Matching Registered Transcripts
NP_002418.1:p.Phe75Ser	CA120433 NM_002427.4:c.224T>C