Canonical Allele Identifier: PA2826877129
Gene: MYT1L HGNC NCBI

Linked Data

ClinVar Variation Id: 2575086
ClinVar RCV Id: RCV003320011
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001289981.1:p.Cys511Tyr
CA345702056
NM_001303052.2:c.1532G>A