Canonical Allele Identifier: PA238906
Gene: WDPCP HGNC NCBI

Linked Data

ClinVar Variation Id: 193387
ClinVar RCV Id: RCV000173453 RCV001247524 RCV002516587 RCV003407639
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_056994.3:p.Phe5Leu
CA238905
NM_015910.7:c.13T>C
CA347066638
NM_015910.7:c.15T>G
CA347066639
NM_015910.7:c.15T>A