Canonical Allele Identifier: PA2828327392
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143393

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356322.1:p.Pro295Ser
CA274535
NM_001369393.2:c.883C>T