Canonical Allele Identifier: PA915958311
Gene: F8 HGNC NCBI

Linked Data

ClinVar Variation Id: 627191
ClinVar RCV Id: RCV000851962

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000123.1:p.Glu340Asp
CA414917333
NM_000132.4:c.1020A>T
CA414917341
NM_000132.4:c.1020A>C