Canonical Allele Identifier: PA2826918406
Gene: WDSUB1 HGNC NCBI
ClinVar Allele:
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001294923.1:p.His67Leu
CA348918998
NM_001307994.2:c.200A>T