Canonical Allele Identifier: PA1139721003
Gene: DMD HGNC NCBI

Linked Data

ClinVar Variation Id: 913633

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004002.3:p.Leu307Val
CA10378816
NM_004011.4:c.919T>G