Canonical Allele Identifier: PA645435781
Gene: TSFM HGNC NCBI

Linked Data

ClinVar Variation Id: 418526
ClinVar RCV Id: RCV000486103 RCV002526516 RCV001109601
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001166167.1:p.Ser236Phe
CA6659423
NM_001172696.2:c.707C>T