Canonical Allele Identifier: PA2826379448
Gene: MYPN HGNC NCBI

Linked Data

ClinVar Variation Id: 1981608
ClinVar RCV Id: RCV002751564
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243196.1:p.Arg1044Leu
CA376857584
NM_001256267.2:c.3131G>T