Canonical Allele Identifier: PA2829629988
Gene: TSFM HGNC NCBI

Linked Data

ClinVar Variation Id: 2169960
ClinVar RCV Id: RCV003085094

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005717.3:p.Glu314Gly
CA6659481
NM_005726.6:c.941A>G