Canonical Allele Identifier: PA916070095
Gene: MYPN HGNC NCBI

Linked Data

ClinVar Variation Id: 640837
ClinVar RCV Id: RCV000793944 RCV002397574
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_115967.2:p.Glu566Gln
CA376839794
NM_032578.4:c.1696G>C