Canonical Allele Identifier: PA2826379956
Gene: MYPN HGNC NCBI

Linked Data

ClinVar Variation Id: 1782197
ClinVar RCV Id: RCV002408152
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243197.1:p.Asn339Ser
CA376840690
NM_001256268.2:c.1016A>G