Canonical Allele Identifier: PA658654973
Gene: MSL2 HGNC NCBI

Linked Data

ClinVar Variation Id: 440996
ClinVar RCV Id: RCV000509141

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060603.2:p.Pro25Ser
CA2631499
NM_018133.4:c.73C>T