Canonical Allele Identifier: PA2580483632
Gene: MYPN HGNC NCBI

Linked Data

ClinVar Variation Id: 2049015
ClinVar RCV Id: RCV002932176
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_115967.2:p.Pro651Thr
CA376841051
NM_032578.4:c.1951C>A