Canonical Allele Identifier: PA913191691
Gene: F8 HGNC NCBI

Linked Data

ClinVar Variation Id: 618634
ClinVar RCV Id: RCV000757246

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000123.1:p.Ser1806Phe
CA414908914
NM_000132.4:c.5417C>T