Canonical Allele Identifier: PA2826379463
Gene: MYPN HGNC NCBI

Linked Data

ClinVar Variation Id: 417954
ClinVar RCV Id: RCV000477765 RCV001564719 RCV002489140 RCV002323814
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243196.1:p.Arg1057Gln
CA5522981
NM_001256267.2:c.3170G>A