Canonical Allele Identifier: PA2826379521
Gene: MYPN HGNC NCBI

Linked Data

ClinVar Variation Id: 1369823
ClinVar RCV Id: RCV001894984
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243196.1:p.His1129Asn
CA208226042
NM_001256267.2:c.3385C>A