Allele Registry

Canonical Allele Identifier: PA103198

Gene: F11 HGNC NCBI

ClinVar Allele:

26939

ClinVar RCV:

RCV000012675

ClinVar Variation:

11900

HGVS (amino-acid)	Matching Registered Transcripts
NP_000119.1:p.Ser594Arg	CA121761 NM_000128.4:c.1782C>A CA358946072 NM_000128.4:c.1780A>C CA358946080 NM_000128.4:c.1782C>G