Canonical Allele Identifier: PA2828325187
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1315124
ClinVar RCV Id: RCV001773318

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356320.1:p.Ala88Ser
CA415173789
NM_001369391.2:c.262G>T