Canonical Allele Identifier: PA2580515086
Gene: MTFMT HGNC NCBI

Linked Data

ClinVar Variation Id: 2210992
ClinVar RCV Id: RCV002677033
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_640335.2:p.Pro11Leu
CA271504873
NM_139242.4:c.32C>T