Canonical Allele Identifier: PA916009757
Gene: MIPEP HGNC NCBI

Linked Data

ClinVar Variation Id: 208633
ClinVar RCV Id: RCV000412519 RCV000605166
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005923.3:p.His512Asp
CA6912972
NM_005932.4:c.1534C>G