Canonical Allele Identifier: PA2741862477
Gene: MYT1L HGNC NCBI

Linked Data

ClinVar Variation Id: 2575086
ClinVar RCV Id: RCV003320011
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001316780.1:p.Cys511Tyr
CA345702056
NM_001329851.3:c.1532G>A