Canonical Allele Identifier: PA2825968639
Gene: ENTPD1 HGNC NCBI

Linked Data

ClinVar Variation Id: 498850
ClinVar RCV Id: RCV000595576 RCV001484653 RCV001848982
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157651.1:p.Ile452Met
CA5621667
NM_001164179.1:c.1356C>G