Canonical Allele Identifier: PA2829069314
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143344

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001373067.1:p.Val157Met
CA199319
NM_001386138.1:c.469G>A