Canonical Allele Identifier: PA2827272273
Gene: MYT1L HGNC NCBI

Linked Data

ClinVar Variation Id: 375549
ClinVar RCV Id: RCV000416999

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001316773.1:p.Leu520Pro
CA16044342
NM_001329844.2:c.1559T>C