Canonical Allele Identifier: PA2826379661
Gene: MYPN HGNC NCBI

Linked Data

ClinVar Variation Id: 544039
ClinVar RCV Id: RCV000655044 RCV004025947
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243196.1:p.Arg1278Trp
CA376829942
NM_001256267.2:c.3832C>T