Canonical Allele Identifier: PA2741891873
Gene: DSG2 HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001934.2:p.Tyr1117Phe
CA402149559
NM_001943.5:c.3350A>T