Canonical Allele Identifier: PA1139670697
Gene: F8 HGNC NCBI

Linked Data

ClinVar Variation Id: 993916
ClinVar RCV Id: RCV001286176
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000123.1:p.Glu2341Lys
CA414896766
NM_000132.4:c.7021G>A