Canonical Allele Identifier: PA2826379014
Gene: MYPN HGNC NCBI

Linked Data

ClinVar Variation Id: 477741
ClinVar RCV Id: RCV000553767 RCV002395491
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243196.1:p.Asp537Tyr
CA5522627
NM_001256267.2:c.1609G>T