Allele Registry

Canonical Allele Identifier: PA186147

Gene: MMP13 HGNC NCBI

ClinVar RCV:

RCV000162347

RCV000303456

RCV004019951

ClinVar Variation:

183687

HGVS (amino-acid)	Matching Registered Transcripts
NP_002418.1:p.Trp207Gly	CA186146 NM_002427.4:c.619T>G