Allele Registry

Canonical Allele Identifier: PA2741966025

Gene: F8 HGNC NCBI

ClinVar RCV:

RCV003393027

ClinVar Variation:

2635321

HGVS (amino-acid)	Matching Registered Transcripts
NP_063916.1:p.Ser57Arg	CA414906517 NM_019863.3:c.171T>G CA414906518 NM_019863.3:c.171T>A CA414906786 NM_019863.3:c.169A>C