Canonical Allele Identifier: PA916070111
Gene: MYPN HGNC NCBI

Linked Data

ClinVar Variation Id: 684786
ClinVar RCV Id: RCV000845330
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_115967.2:p.Thr620Ser
CA376840491
NM_032578.4:c.1858A>T
CA376840505
NM_032578.4:c.1859C>G