Canonical Allele Identifier: PA2827293172
Gene: WDSUB1 HGNC NCBI
ClinVar Allele:
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317203.1:p.His67Leu
CA348918998
NM_001330274.2:c.200A>T