Canonical Allele Identifier: PA2829565099
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1923631

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004983.1:p.Pro199Thr
CA10558584
NM_004992.4:c.595C>A