Allele Registry

Canonical Allele Identifier: PA121878

Gene: F7 HGNC NCBI

ClinVar RCV:

RCV000012871

ClinVar Variation:

12090

HGVS (amino-acid)	Matching Registered Transcripts
NP_000122.1:p.Phe328Ser	CA121874 NM_000131.4:c.983T>C