Canonical Allele Identifier: PA645502001
Gene: MYT1L HGNC NCBI

Linked Data

ClinVar Variation Id: 375549
ClinVar RCV Id: RCV000416999
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001289981.1:p.Leu520Pro
CA16044342
NM_001303052.2:c.1559T>C