Canonical Allele Identifier: PA2829794627
Gene: MYT1L HGNC NCBI

Linked Data

ClinVar Variation Id: 235469
ClinVar RCV Id: RCV000224698 RCV000754090 RCV001257695
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055840.2:p.Arg567Gln
CA10581322
NM_015025.4:c.1700G>A