Allele Registry

Canonical Allele Identifier: PA2826943681

Gene: F10 HGNC NCBI

ClinVar RCV:

RCV000012833

ClinVar Variation:

12053

HGVS (amino-acid)	Matching Registered Transcripts
NP_001299603.1:p.Arg322Cys	CA121837 NM_001312674.2:c.964C>T