Canonical Allele Identifier: PA645435787
Gene: TSFM HGNC NCBI

Linked Data

ClinVar Variation Id: 310018
ClinVar RCV Id: RCV000381575 RCV000874485 RCV001277411 RCV003957607
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001166167.1:p.Arg275Cys
CA6659439
NM_001172696.2:c.823C>T