Canonical Allele Identifier: PA916039418
Gene: F11 HGNC NCBI

Linked Data

ClinVar Variation Id: 68176
ClinVar RCV Id: RCV000059008

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341733.1:p.Cys46Phe
CA219108
NM_001354804.2:c.137G>T