Canonical Allele Identifier: PA170326
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143618
ClinVar RCV Id: RCV000133158 RCV003990991
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004983.1:p.Gly183Arg
CA170325
NM_004992.4:c.547G>C
CA415173745
NM_004992.4:c.547G>A