Canonical Allele Identifier: PA2828325796
Gene: MECP2 HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356320.1:p.Ala353Val
CA10558438
NM_001369391.2:c.1058C>T