Canonical Allele Identifier: PA2741830549
Gene: MECP2 HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001104262.1:p.Ala456del
CA2466570163
NM_001110792.2:c.1366_1368del