Allele Registry

Canonical Allele Identifier: PA109058

Gene: F8 HGNC NCBI

ClinVar RCV:

RCV000010890

RCV000851946

RCV001701720

RCV003398478

ClinVar Variation:

10177

HGVS (amino-acid)	Matching Registered Transcripts
NP_000123.1:p.Val181Met	CA255066 NM_000132.4:c.541G>A