Allele Registry

Canonical Allele Identifier: PA121849

Gene: F7 HGNC NCBI

ClinVar Allele:

27114

ClinVar RCV:

RCV000012856

ClinVar Variation:

12075

HGVS (amino-acid)	Matching Registered Transcripts
NP_062562.1:p.Leu13Pro	CA121846 NM_019616.4:c.38T>C