Allele Registry

Canonical Allele Identifier: PA2826688564

Gene: ANLN HGNC NCBI

ClinVar RCV:

RCV000144242

ClinVar Variation:

156221

HGVS (amino-acid)	Matching Registered Transcripts
NP_001271231.1:p.Arg431Cys	CA170791 NM_001284302.3:c.1291C>T