Canonical Allele Identifier: PA2827272532
Gene: MYT1L HGNC NCBI

Linked Data

ClinVar Variation Id: 975749
ClinVar RCV Id: RCV001252575 RCV001586091
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001316774.1:p.Cys506Arg
CA345702090
NM_001329845.1:c.1516T>C