Canonical Allele Identifier: PA105313
Gene: F8 HGNC NCBI

Linked Data

ClinVar Variation Id: 10140
ClinVar RCV Id: RCV000010853
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000123.1:p.Asn1941Asp
CA255033
NM_000132.4:c.5821A>G