Allele Registry

Canonical Allele Identifier: PA2580194358

Gene: SEPTIN11 HGNC NCBI

ClinVar RCV:

RCV004272643

ClinVar Variation:

2484003

HGVS (amino-acid)	Matching Registered Transcripts
NP_001293076.1:p.Met259Ile	CA357454935 NM_001306147.2:c.777G>A CA357454936 NM_001306147.2:c.777G>C CA357454937 NM_001306147.2:c.777G>T