Canonical Allele Identifier: PA2829565427
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 655951

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004983.1:p.Pro361Ser
CA415168076
NM_004992.4:c.1081C>T