Canonical Allele Identifier: PA2826379954
Gene: MYPN HGNC NCBI

Linked Data

ClinVar Variation Id: 1488943
ClinVar RCV Id: RCV001980382
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243197.1:p.Arg337Gly
CA376840650
NM_001256268.2:c.1009A>G