Canonical Allele Identifier: PA2826379955
Gene: MYPN HGNC NCBI

Linked Data

ClinVar Variation Id: 379702

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243197.1:p.Arg337Lys
CA16606036
NM_001256268.2:c.1010G>A