Canonical Allele Identifier: PA2826379933
Gene: MYPN HGNC NCBI

Linked Data

ClinVar Variation Id: 2563976
ClinVar RCV Id: RCV003306305
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243197.1:p.Gly322Val
CA208192861
NM_001256268.2:c.965G>T