Canonical Allele Identifier: PA2829565156
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1373281
ClinVar RCV Id: RCV001900325

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004983.1:p.Pro230Ala
CA415172534
NM_004992.4:c.688C>G