Canonical Allele Identifier: PA2580180370
Gene: MYPN HGNC NCBI

Linked Data

ClinVar Variation Id: 2412857
ClinVar RCV Id: RCV003109872
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243197.1:p.Val742Ile
CA376857415
NM_001256268.2:c.2224G>A