Canonical Allele Identifier: PA2826380300
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_001243197.1:p.Gln844Leu
CA376859272
NM_001256268.2:c.2531A>T