Canonical Allele Identifier: PA2573220639
Gene: MMP13 HGNC NCBI

Linked Data

ClinVar Variation Id: 1511466
ClinVar RCV Id: RCV002043338
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002418.1:p.Arg109Leu
CA6252022
NM_002427.4:c.326G>T