Canonical Allele Identifier: PA108161
Gene: ENPP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 13588
ClinVar RCV Id: RCV000014557

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006199.2:p.Leu579Phe
CA256905
NM_006208.3:c.1737G>C
CA365651814
NM_006208.3:c.1737G>T