Canonical Allele Identifier: PA2499242972
Gene: MYPN HGNC NCBI

Linked Data

ClinVar Variation Id: 1043882
ClinVar RCV Id: RCV001348054
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243197.1:p.Gly755Arg
CA5522958
NM_001256268.2:c.2263G>C