Canonical Allele Identifier: PA2827272270
Gene: MYT1L HGNC NCBI

Linked Data

ClinVar Variation Id: 1697307
ClinVar RCV Id: RCV002267689
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001316773.1:p.Gly513Val
CA345702038
NM_001329844.2:c.1538G>T