Canonical Allele Identifier: PA2826379942
Gene: MYPN HGNC NCBI

Linked Data

ClinVar Variation Id: 2010576
ClinVar RCV Id: RCV002834086

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243197.1:p.Thr329Ser
CA5522671
NM_001256268.2:c.985A>T
CA376840543
NM_001256268.2:c.986C>G