Canonical Allele Identifier: PA2826378568
Gene: MYPN HGNC NCBI

Linked Data

ClinVar Variation Id: 229028
ClinVar RCV Id: RCV000213132 RCV001234753 RCV002503859
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243196.1:p.Glu18Asp
CA10576796
NM_001256267.2:c.54G>C
CA377103513
NM_001256267.2:c.54G>T