Canonical Allele Identifier: PA2829501549
Gene: DMD HGNC NCBI

Linked Data

ClinVar Variation Id: 1064318
ClinVar RCV Id: RCV001374271
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004003.2:p.Leu298Phe
CA412672151
NM_004012.4:c.894G>T
CA412672153
NM_004012.4:c.894G>C