Allele Registry

Canonical Allele Identifier: PA658825423

Gene: F11 HGNC NCBI

ClinVar RCV:

RCV000674279

ClinVar Variation:

558063

HGVS (amino-acid)	Matching Registered Transcripts
NP_000119.1:p.Ile215_Asp216del	CA557396098 NM_000128.4:c.644_649del