Canonical Allele Identifier: PA2573220635
Gene: MMP13 HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

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