Canonical Allele Identifier: PA2827272538
Gene: MYT1L HGNC NCBI

Linked Data

ClinVar Variation Id: 375549
ClinVar RCV Id: RCV000416999
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001316774.1:p.Leu520Pro
CA16044342
NM_001329845.1:c.1559T>C