Allele Registry

Canonical Allele Identifier: PA3057313076

Gene: F8 HGNC NCBI

ClinVar RCV:

RCV004812531

ClinVar Variation:

3390360

HGVS (amino-acid)	Matching Registered Transcripts
NP_000123.1:p.Ile405Thr	CA414916092 NM_000132.4:c.1214T>C