Canonical Allele Identifier: PA2829068402
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143657

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001373066.1:p.Thr5Ser
CA172571
NM_001386137.1:c.14C>G
CA415172595
NM_001386137.1:c.13A>T