Canonical Allele Identifier: PA2826877130
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_001289981.1:p.Gly513Val
CA345702038
NM_001303052.2:c.1538G>T