Allele Registry

Canonical Allele Identifier: PA096971

Gene: F10 HGNC NCBI

ClinVar RCV:

RCV000012833

ClinVar Variation:

12053

HGVS (amino-acid)	Matching Registered Transcripts
NP_000495.1:p.Arg366Cys	CA121837 NM_000504.4:c.1096C>T