Allele Registry

Canonical Allele Identifier: PA103785

Gene: F7 HGNC NCBI

ClinVar RCV:

RCV000012866

ClinVar Variation:

12085

HGVS (amino-acid)	Matching Registered Transcripts
NP_000122.1:p.Cys389Gly	CA121860 NM_000131.4:c.1165T>G