Canonical Allele Identifier: PA2826943272
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_001299583.1:p.Ile385Met
CA5621667
NM_001312654.1:c.1155C>G