ClinGen Allele Registry
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Canonical Allele Identifier:
PA2827293172
Gene: WDSUB1
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar Allele:
2299603
ClinVar RCV:
RCV004154923
ClinVar Variation:
2304646
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001317203.1:p.His67Leu
CA348918998
NM_001330274.2:c.200A>T