Canonical Allele Identifier: PA143768
Gene: MYPN HGNC NCBI

Linked Data

ClinVar Variation Id: 31792
ClinVar RCV Id: RCV000024485 RCV000043543 RCV000219549 RCV000621596 RCV003989299
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_115967.2:p.Val1195Met
CA143766
NM_032578.4:c.3583G>A