Canonical Allele Identifier: PA102938
Gene: F11 HGNC NCBI

Linked Data

ClinVar Variation Id: 68176
ClinVar RCV Id: RCV000059008
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000119.1:p.Cys46Phe
CA219108
NM_000128.4:c.137G>T