Canonical Allele Identifier: PA2826378561
Gene: MYPN HGNC NCBI

Linked Data

ClinVar Variation Id: 222747
ClinVar RCV Id: RCV000208248 RCV002515548 RCV003380519
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243196.1:p.Ile12Thr
CA351882
NM_001256267.2:c.35T>C