Canonical Allele Identifier: PA645507070
Gene: MYPN HGNC NCBI

Linked Data

ClinVar Variation Id: 379702
ClinVar RCV Id: RCV001703564 RCV001851050
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_115967.2:p.Arg631Lys
CA16606036
NM_032578.4:c.1892G>A