Canonical Allele Identifier: PA645479625
Gene: MMP13 HGNC NCBI

Linked Data

ClinVar Variation Id: 301990
ClinVar RCV Id: RCV000312854 RCV000402601 RCV001322935
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002418.1:p.Val101Leu
CA6252030
NM_002427.4:c.301G>T
CA382232314
NM_002427.4:c.301G>C