Canonical Allele Identifier: PA343870
Gene: F8 HGNC NCBI

Linked Data

ClinVar Variation Id: 41001

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000123.1:p.Met2257Val
CA343869
NM_000132.4:c.6769A>G