Canonical Allele Identifier: PA915958533
Gene: F8 HGNC NCBI

Linked Data

ClinVar Variation Id: 627338
ClinVar RCV Id: RCV000852163

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000123.1:p.Met1966Leu
CA414906143
NM_000132.4:c.5896A>T
CA414906151
NM_000132.4:c.5896A>C