Canonical Allele Identifier: PA2580229386
Gene: F11 HGNC NCBI

Linked Data

ClinVar Variation Id: 1704969
ClinVar RCV Id: RCV002283296
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341733.1:p.Asp69Gly
CA112149165
NM_001354804.2:c.206A>G