Canonical Allele Identifier: PA2829496940
Gene: DMD HGNC NCBI

Linked Data

ClinVar Variation Id: 497119
ClinVar RCV Id: RCV000592278 RCV002530962 RCV003302907
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004001.1:p.Lys1311Asn
CA10378993
NM_004010.3:c.3933G>C
CA412664012
NM_004010.3:c.3933G>T