Canonical Allele Identifier: PA105638
Gene: F8 HGNC NCBI

Linked Data

ClinVar Variation Id: 10179
ClinVar RCV Id: RCV000010892
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000123.1:p.Asp222Val
CA255068
NM_000132.4:c.665A>T