Canonical Allele Identifier: PA2826379124
Gene: MYPN HGNC NCBI

Linked Data

ClinVar Variation Id: 1368486
ClinVar RCV Id: RCV001874424

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243196.1:p.Lys657Arg
CA376841161
NM_001256267.2:c.1970A>G