Canonical Allele Identifier: PA2826379098
Gene: MYPN HGNC NCBI

Linked Data

ClinVar Variation Id: 1781883
ClinVar RCV Id: RCV002415300
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243196.1:p.Ser627Tyr
CA376840612
NM_001256267.2:c.1880C>A