Canonical Allele Identifier: PA2573078697
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 11841

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001373068.1:p.Pro2Leu
CA121713
NM_001386139.1:c.5C>T