Canonical Allele Identifier: PA2573078763
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143749

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001373068.1:p.Arg86Trp
CA199325
NM_001386139.1:c.256C>T