Canonical Allele Identifier: PA2573220635
Gene: MMP13 HGNC NCBI

Linked Data

ClinVar Variation Id: 1507065
ClinVar RCV Id: RCV002038266
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002418.1:p.Asn105Ser
CA382232223
NM_002427.4:c.314A>G