Allele Registry

Canonical Allele Identifier: PA103147

Gene: F11 HGNC NCBI

ClinVar RCV:

RCV000169580

ClinVar Variation:

189154

HGVS (amino-acid)	Matching Registered Transcripts
NP_000119.1:p.Pro538Leu	CA199131 NM_000128.4:c.1613C>T