Canonical Allele Identifier: PA916009773
Gene: MIPEP HGNC NCBI

Linked Data

ClinVar Variation Id: 392943
ClinVar RCV Id: RCV000432045 RCV001335345
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005923.3:p.Gly682Asp
CA6912678
NM_005932.4:c.2045G>A