Canonical Allele Identifier: PA2827274022
Gene: MYT1L HGNC NCBI

Linked Data

ClinVar Variation Id: 975749
ClinVar RCV Id: RCV001252575 RCV001586091
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001316781.1:p.Cys504Arg
CA345702090
NM_001329852.3:c.1510T>C