Canonical Allele Identifier: PA2829629752
Gene: TSFM HGNC NCBI

Linked Data

ClinVar Variation Id: 310017

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005717.3:p.Val230Leu
CA6659430
NM_005726.6:c.688G>T
CA385530517
NM_005726.6:c.688G>C