Canonical Allele Identifier: PA645389725
Gene: MTFMT HGNC NCBI

Linked Data

ClinVar Variation Id: 418337
ClinVar RCV Id: RCV000480605

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_640335.2:p.Leu223Phe
CA7613280
NM_139242.4:c.669G>T
CA392852573
NM_139242.4:c.669G>C