Canonical Allele Identifier: PA103296
Gene: F11 HGNC NCBI

Linked Data

ClinVar Variation Id: 11904
ClinVar RCV Id: RCV000012679

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000119.1:p.Trp587Ser
CA121769
NM_000128.4:c.1760G>C