Canonical Allele Identifier: PA2829491789
Gene: DMD HGNC NCBI

Linked Data

ClinVar Variation Id: 2173940
ClinVar RCV Id: RCV002584851

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004000.1:p.Lys1705Asn
CA412671467
NM_004009.3:c.5115A>C
CA412671468
NM_004009.3:c.5115A>T