Canonical Allele Identifier: PA2827273079
Gene: MYT1L HGNC NCBI

Linked Data

ClinVar Variation Id: 235469
ClinVar RCV Id: RCV000224698 RCV000754090 RCV001257695
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001316776.1:p.Arg567Gln
CA10581322
NM_001329847.2:c.1700G>A