Canonical Allele Identifier: PA170246
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143475

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004983.1:p.Ser477Thr
CA170245
NM_004992.4:c.1430G>C