Canonical Allele Identifier: PA2741810483
Gene: F9 HGNC NCBI

Linked Data

ClinVar Variation Id: 2636137
ClinVar RCV Id: RCV003402867

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000124.1:p.Glu286Asp
CA414444527
NM_000133.4:c.858G>C
CA414444530
NM_000133.4:c.858G>T