Allele Registry

Canonical Allele Identifier: PA097320

Gene: F12 HGNC NCBI

ClinVar RCV:

RCV000778921

RCV001158012

ClinVar Variation:

1168

HGVS (amino-acid)	Matching Registered Transcripts
NP_000496.2:p.Tyr53Cys	CA114815 NM_000505.4:c.158A>G