Canonical Allele Identifier: PA2826955934
Gene: MECP2 HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001303266.1:p.Pro209Thr
CA270562
NM_001316337.2:c.625C>A