Canonical Allele Identifier: PA2829507934
Gene: DMD HGNC NCBI

Linked Data

ClinVar Variation Id: 2440844
ClinVar RCV Id: RCV003146145
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004010.1:p.Phe131Leu
CA328407915
NM_004019.3:c.393T>A
CA412649534
NM_004019.3:c.393T>G
CA412649541
NM_004019.3:c.391T>C