Canonical Allele Identifier: PA2826379095
Gene: MYPN HGNC NCBI

Linked Data

ClinVar Variation Id: 691723
ClinVar RCV Id: RCV000852611 RCV001858511 RCV002409008 RCV003442123
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243196.1:p.Asp626Asn
CA5522672
NM_001256267.2:c.1876G>A