Canonical Allele Identifier: PA2826379437
Gene: MYPN HGNC NCBI

Linked Data

ClinVar Variation Id: 1727538
ClinVar RCV Id: RCV002325878 RCV003102307
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243196.1:p.His1033Gln
CA376857375
NM_001256267.2:c.3099C>A
CA376857377
NM_001256267.2:c.3099C>G