Canonical Allele Identifier: PA645435783
Gene: TSFM HGNC NCBI

Linked Data

ClinVar Variation Id: 310017

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001166167.1:p.Val251Leu
CA6659430
NM_001172696.2:c.751G>T
CA385530517
NM_001172696.2:c.751G>C