Canonical Allele Identifier: PA658812178
Gene: MYPN HGNC NCBI

Linked Data

ClinVar Variation Id: 31800
ClinVar RCV Id: RCV000024493 RCV000172772 RCV000252665 RCV000625362 RCV001778667
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243197.1:p.Pro841Thr
CA200038
NM_001256268.2:c.2521C>A