Canonical Allele Identifier: PA2573162410
Gene: F8 HGNC NCBI

Linked Data

ClinVar Variation Id: 1685781
ClinVar RCV Id: RCV002249948

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000123.1:p.Asp2317Glu
CA10567727
NM_000132.4:c.6951C>G
CA414897405
NM_000132.4:c.6951C>A