Allele Registry

Canonical Allele Identifier: PA105378

Gene: MMP13 HGNC NCBI

ClinVar RCV:

RCV000010051

ClinVar Variation:

9444

HGVS (amino-acid)	Matching Registered Transcripts
NP_002418.1:p.Phe74Ser	CA120434 NM_002427.4:c.221T>C