Allele Registry

Canonical Allele Identifier: PA2826500818

Gene: F7 HGNC NCBI

ClinVar RCV:

RCV000012866

ClinVar Variation:

12085

HGVS (amino-acid)	Matching Registered Transcripts
NP_001254483.1:p.Cys305Gly	CA121860 NM_001267554.1:c.913T>G