Canonical Allele Identifier: PA2825667103
Gene: WDSUB1 HGNC NCBI
ClinVar Allele:
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121684.1:p.His67Leu
CA348918998
NM_001128212.3:c.200A>T