Canonical Allele Identifier: PA2829069540
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2826707
ClinVar RCV Id: RCV003639914
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001373067.1:p.Val252Leu
CA415163239
NM_001386138.1:c.754G>T
CA415163240
NM_001386138.1:c.754G>C