Allele Registry

Canonical Allele Identifier: PA2829694200

Gene: PEMT HGNC NCBI

ClinVar RCV:

RCV001693056

ClinVar Variation:

1279483

HGVS (amino-acid)	Matching Registered Transcripts
NP_009100.2:p.Val175Met	CA8417709 NM_007169.3:c.523G>A