Canonical Allele Identifier: PA346547
Gene: MYPN HGNC NCBI

Linked Data

ClinVar Variation Id: 180453
ClinVar RCV Id: RCV000157387 RCV000476557 RCV001311707 RCV002372026 RCV002492609
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243196.1:p.Met1305Val
CA346545
NM_001256267.2:c.3913A>G