Canonical Allele Identifier: PA2499267695
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 1009716

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004406.2:p.Met266Leu
CA362674001
NM_004415.4:c.796A>C
CA362674004
NM_004415.4:c.796A>T