Canonical Allele Identifier: PA2826379936
Gene: MYPN HGNC NCBI

Linked Data

ClinVar Variation Id: 191751
ClinVar RCV Id: RCV000172073 RCV000655038 RCV002408748
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243197.1:p.Thr326Ala
CA237454
NM_001256268.2:c.976A>G