Canonical Allele Identifier: PA2827273590
Gene: MYT1L HGNC NCBI

Linked Data

ClinVar Variation Id: 2575086
ClinVar RCV Id: RCV003320011
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001316778.1:p.Cys509Tyr
CA345702056
NM_001329849.3:c.1526G>A