Canonical Allele Identifier: PA2825968927
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_001157655.1:p.Ile355Met
CA5621667
NM_001164183.2:c.1065C>G