Canonical Allele Identifier: PA121127
Gene: F9 HGNC NCBI

Linked Data

ClinVar Variation Id: 10588

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000124.1:p.Thr194Ala
CA121125
NM_000133.4:c.580A>G