Allele Registry

Canonical Allele Identifier: PA2829901362

Gene: SEPTIN11 HGNC NCBI

ClinVar RCV:

RCV004272643

ClinVar Variation:

2484003

HGVS (amino-acid)	Matching Registered Transcripts
NP_060713.1:p.Met249Ile	CA357454935 NM_018243.4:c.747G>A CA357454936 NM_018243.4:c.747G>C CA357454937 NM_018243.4:c.747G>T