Canonical Allele Identifier: PA2826379082
Gene: MYPN HGNC NCBI

Linked Data

ClinVar Variation Id: 3228157
ClinVar RCV Id: RCV004519867
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243196.1:p.Ala615Thr
CA376840431
NM_001256267.2:c.1843G>A