Canonical Allele Identifier: PA108116
Gene: ENPP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 88752
ClinVar RCV Id: RCV000074403

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006199.2:p.Cys149Ser
CA145332
NM_006208.3:c.446G>C
CA365661065
NM_006208.3:c.445T>A