Allele Registry

Canonical Allele Identifier: PA210742

Gene: F13B HGNC NCBI

ClinVar RCV:

RCV000017984

RCV000253350

RCV000301691

RCV001642228

ClinVar Variation:

16520

HGVS (amino-acid)	Matching Registered Transcripts
NP_001985.2:p.Arg115His	CA210740 NM_001994.3:c.344G>A