Canonical Allele Identifier: PA2825073989
Gene: DMD HGNC NCBI

Linked Data

ClinVar Variation Id: 598379
ClinVar RCV Id: RCV000734758 RCV000807737 RCV001825485
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000100.3:p.Trp2477Cys
CA10378272
NM_000109.4:c.7431G>T
CA412658894
NM_000109.4:c.7431G>C