Allele Registry

Canonical Allele Identifier: PA2573061397

Gene: F8 HGNC NCBI

ClinVar RCV:

RCV001802300

ClinVar Variation:

1330641

HGVS (amino-acid)	Matching Registered Transcripts
NP_000123.1:p.Asp222Ala	CA414919206 NM_000132.4:c.665A>C