Canonical Allele Identifier: PA102878
Gene: F11 HGNC NCBI

Linked Data

ClinVar Variation Id: 68195
ClinVar RCV Id: RCV000059027 RCV000852186
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000119.1:p.Asp222Tyr
CA219144
NM_000128.4:c.664G>T