Canonical Allele Identifier: PA2829506396
Gene: DMD HGNC NCBI

Linked Data

ClinVar Variation Id: 2440844
ClinVar RCV Id: RCV003146145

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004007.1:p.Phe131Leu
CA328407915
NM_004016.3:c.393T>A
CA412649534
NM_004016.3:c.393T>G
CA412649541
NM_004016.3:c.391T>C