Canonical Allele Identifier: PA2826379969
Gene: MYPN HGNC NCBI

Linked Data

ClinVar Variation Id: 647231
ClinVar RCV Id: RCV000801694

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243197.1:p.Pro356Ser
CA5522691
NM_001256268.2:c.1066C>T