Canonical Allele Identifier: PA2829491717
Gene: DMD HGNC NCBI

Linked Data

ClinVar Variation Id: 1395206
ClinVar RCV Id: RCV001891327
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004000.1:p.Ala1663Val
CA10378810
NM_004009.3:c.4988C>T