Canonical Allele Identifier: PA2826379937
Gene: MYPN HGNC NCBI

Linked Data

ClinVar Variation Id: 684786
ClinVar RCV Id: RCV000845330
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243197.1:p.Thr326Ser
CA376840491
NM_001256268.2:c.976A>T
CA376840505
NM_001256268.2:c.977C>G