Canonical Allele Identifier: PA645377799
Gene: WDPCP HGNC NCBI

Linked Data

ClinVar Variation Id: 336760
ClinVar RCV Id: RCV000318207 RCV001413862 RCV002519984 RCV003932339
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_056994.3:p.Asp705Tyr
CA1682000
NM_015910.7:c.2113G>T