Allele Registry

Canonical Allele Identifier: PA2826500759

Gene: F7 HGNC NCBI

ClinVar RCV:

RCV000012871

ClinVar Variation:

12090

HGVS (amino-acid)	Matching Registered Transcripts
NP_001254483.1:p.Phe244Ser	CA121874 NM_001267554.1:c.731T>C