Canonical Allele Identifier: PA1139719548
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 919144

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004406.2:p.Met2047Ile
CA046950
NM_004415.4:c.6141G>C
CA362690166
NM_004415.4:c.6141G>A
CA362690167
NM_004415.4:c.6141G>T