Allele Registry

Canonical Allele Identifier: PA2741810311

Gene: F8 HGNC NCBI

ClinVar RCV:

RCV003412221

ClinVar Variation:

2629508

HGVS (amino-acid)	Matching Registered Transcripts
NP_000123.1:p.Ala119Pro	CA414919938 NM_000132.4:c.355G>C