Canonical Allele Identifier: PA916009756
Gene: MIPEP HGNC NCBI

Linked Data

ClinVar Variation Id: 208632
ClinVar RCV Id: RCV000412622 RCV000616524
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005923.3:p.Lys343Glu
CA16040611
NM_005932.4:c.1027A>G