Canonical Allele Identifier: PA2826379078
Gene: MYPN HGNC NCBI

Linked Data

ClinVar Variation Id: 2683107
ClinVar RCV Id: RCV003481974
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243196.1:p.Ser613Phe
CA376840419
NM_001256267.2:c.1838C>T