Canonical Allele Identifier: PA2826379948
Gene: MYPN HGNC NCBI

Linked Data

ClinVar Variation Id: 520317
ClinVar RCV Id: RCV000618459 RCV001231665
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243197.1:p.Ser333Thr
CA376840605
NM_001256268.2:c.997T>A