Canonical Allele Identifier: PA2825797232
Gene: CTF1 HGNC NCBI

Linked Data

ClinVar Variation Id: 163017

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001136016.1:p.Ala91Glu
CA175614
NM_001142544.3:c.272C>A