Canonical Allele Identifier: PA2580483626
Gene: MYPN HGNC NCBI

Linked Data

ClinVar Variation Id: 2010576
ClinVar RCV Id: RCV002834086
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_115967.2:p.Thr623Ser
CA5522671
NM_032578.4:c.1867A>T
CA376840543
NM_032578.4:c.1868C>G