Canonical Allele Identifier: PA103078
Gene: F11 HGNC NCBI

Linked Data

ClinVar Variation Id: 68190
ClinVar RCV Id: RCV000059022 RCV003905028
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000119.1:p.Ile618Ser
CA219134
NM_000128.4:c.1853T>G