Canonical Allele Identifier: PA2829501179
Gene: DMD HGNC NCBI

Linked Data

ClinVar Variation Id: 94611

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004003.2:p.Leu21Phe
CA285566
NM_004012.4:c.61C>T