Canonical Allele Identifier: PA645294915
Gene: F11 HGNC NCBI

Linked Data

ClinVar Variation Id: 371565

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000119.1:p.Cys416Tyr
CA3163932
NM_000128.4:c.1247G>A