Canonical Allele Identifier: PA2826380369
Gene: MYPN HGNC NCBI

Linked Data

ClinVar Variation Id: 1047446
ClinVar RCV Id: RCV001352157 RCV002486460
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243197.1:p.Ser1014Leu
CA5523189
NM_001256268.2:c.3041C>T