Canonical Allele Identifier: PA2826379947
Gene: MYPN HGNC NCBI

Linked Data

ClinVar Variation Id: 1305457
ClinVar RCV Id: RCV001768664 RCV002414307
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243197.1:p.Ser333Phe
CA376840614
NM_001256268.2:c.998C>T