Allele Registry

Canonical Allele Identifier: PA2499228739

Gene: F9 HGNC NCBI

ClinVar RCV:

RCV001382696

ClinVar Variation:

1070514

HGVS (amino-acid)	Matching Registered Transcripts
NP_000124.1:p.Trp453Ter	CA2695236423 NM_000133.4:c.1359del