Canonical Allele Identifier: PA2826379527
Gene: MYPN HGNC NCBI

Linked Data

ClinVar Variation Id: 3228170
ClinVar RCV Id: RCV004519880
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243196.1:p.Gln1138Leu
CA376859272
NM_001256267.2:c.3413A>T