Allele Registry

Canonical Allele Identifier: PA105368

Gene: MMP13 HGNC NCBI

ClinVar RCV:

RCV000010052

RCV001851779

ClinVar Variation:

9445

HGVS (amino-acid)	Matching Registered Transcripts
NP_002418.1:p.Met91Thr	CA120435 NM_002427.4:c.272T>C