Canonical Allele Identifier: PA172599
Gene: MTM1 HGNC NCBI

Linked Data

ClinVar Variation Id: 158952

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000243.1:p.Ile568Val
CA172597
NM_000252.3:c.1702A>G