Canonical Allele Identifier: PA2829513591
Gene: AMPD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2159098
ClinVar RCV Id: RCV003072637

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004028.4:p.Pro512Ser
CA341559206
NM_004037.9:c.1534C>T