Canonical Allele Identifier: PA915958002
Gene: F11 HGNC NCBI

Linked Data

ClinVar Variation Id: 627142
ClinVar RCV Id: RCV000851892
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000119.1:p.Arg268Cys
CA3163785
NM_000128.4:c.802C>T