Canonical Allele Identifier: PA186147
Gene: MMP13 HGNC NCBI

Linked Data

ClinVar Variation Id: 183687
ClinVar RCV Id: RCV000162347 RCV000303456 RCV004019951
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Amino-acid Alleles

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