Canonical Allele Identifier: PA2829907285
Gene: F8 HGNC NCBI

Linked Data

ClinVar Variation Id: 41001

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_063916.1:p.Met122Val
CA343869
NM_019863.3:c.364A>G