Canonical Allele Identifier: PA2829498998
Gene: DMD HGNC NCBI

Linked Data

ClinVar Variation Id: 2440844
ClinVar RCV Id: RCV003146145

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004001.1:p.Phe3076Leu
CA328407915
NM_004010.3:c.9228T>A
CA412649534
NM_004010.3:c.9228T>G
CA412649541
NM_004010.3:c.9226T>C