Canonical Allele Identifier: PA2830275817
Gene: AMPD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2159098
ClinVar RCV Id: RCV003072637
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_631895.1:p.Pro485Ser
CA341559206
NM_139156.4:c.1453C>T