Canonical Allele Identifier: PA2580449126
Gene: MMP27 HGNC NCBI

Linked Data

ClinVar Variation Id: 2368537
ClinVar RCV Id: RCV004205091
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071405.2:p.Phe298Leu
CA6248852
NM_022122.2:c.892T>C
CA382216353
NM_022122.2:c.894T>G
CA382216362
NM_022122.2:c.894T>A