Allele Registry

Canonical Allele Identifier: PA645502003

Gene: MYT1L HGNC NCBI

ClinVar Variation Id: 235469

HGVS (amino-acid)	Matching Registered Transcripts
NP_001289981.1:p.Arg569Gln	CA10581322 NM_001303052.2:c.1706G>A