Canonical Allele Identifier: PA2829069586
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 514317
ClinVar RCV Id: RCV000606712

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001373068.1:p.Thr20Ala
CA10558561
NM_001386139.1:c.58A>G