Allele Registry

Canonical Allele Identifier: PA111001

Gene: AFG3L2 HGNC NCBI

ClinVar RCV:

RCV000005808

ClinVar Variation:

5474

HGVS (amino-acid)	Matching Registered Transcripts
NP_006787.2:p.Asn432Thr	CA340428 NM_006796.3:c.1295A>C