Canonical Allele Identifier: PA105342
Gene: F8 HGNC NCBI

Linked Data

ClinVar Variation Id: 10305
ClinVar RCV Id: RCV000011018

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000123.1:p.Asn2038Ser
CA255198
NM_000132.4:c.6113A>G