Canonical Allele Identifier: PA2826947028
Gene: F9 HGNC NCBI

Linked Data

ClinVar Variation Id: 10607
ClinVar RCV Id: RCV000011353 RCV000792734 RCV000851963 RCV001810849
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001300842.1:p.Thr304Met
CA255381
NM_001313913.2:c.911C>T