Canonical Allele Identifier: PA916027765
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_001316780.1:p.Arg569Gln
CA10581322
NM_001329851.3:c.1706G>A