Canonical Allele Identifier: PA358279
Gene: MYPN HGNC NCBI

Linked Data

ClinVar Variation Id: 31819
ClinVar RCV Id: RCV000024512 RCV000206974 RCV000247848 RCV000216191 RCV000624690 RCV000852614
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243196.1:p.Leu1161Ile
CA215338
NM_001256267.2:c.3481C>A