Canonical Allele Identifier: PA2829794606
Gene: MYT1L HGNC NCBI

Linked Data

ClinVar Variation Id: 1697307
ClinVar RCV Id: RCV002267689
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055840.2:p.Gly511Val
CA345702038
NM_015025.4:c.1532G>T