Allele Registry

Canonical Allele Identifier: PA645294920

Gene: F11 HGNC NCBI

ClinVar RCV:

RCV000411281

RCV001850956

ClinVar Variation:

371214

HGVS (amino-acid)	Matching Registered Transcripts
NP_000119.1:p.Thr593Met	CA3164121 NM_000128.4:c.1778C>T