Canonical Allele Identifier: PA2826379968
Gene: MYPN HGNC NCBI

Linked Data

ClinVar Variation Id: 1015070
ClinVar RCV Id: RCV001313888 RCV004034294
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243197.1:p.Pro355Ala
CA5522688
NM_001256268.2:c.1063C>G