Canonical Allele Identifier: PA2826947094
Gene: F9 HGNC NCBI

Linked Data

ClinVar Variation Id: 1330832
ClinVar RCV Id: RCV001811897
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001300842.1:p.Phe361Ser
CA414446394
NM_001313913.2:c.1082T>C