Canonical Allele Identifier: PA2829069958
Gene: MECP2 HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001373068.1:p.Ala223Val
CA10558438
NM_001386139.1:c.668C>T