Canonical Allele Identifier: PA2830086600
Gene: MYPN HGNC NCBI

Linked Data

ClinVar Variation Id: 2103470
ClinVar RCV Id: RCV003022165
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_115967.2:p.Leu1039Trp
CA376857499
NM_032578.4:c.3116T>G