Canonical Allele Identifier: PA2827273328
Gene: MYT1L HGNC NCBI

Linked Data

ClinVar Variation Id: 375549
ClinVar RCV Id: RCV000416999

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001316777.1:p.Leu518Pro
CA16044342
NM_001329848.1:c.1553T>C