Canonical Allele Identifier: PA916070141
Gene: MYPN HGNC NCBI

Linked Data

ClinVar Variation Id: 647231
ClinVar RCV Id: RCV000801694

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_115967.2:p.Pro650Ser
CA5522691
NM_032578.4:c.1948C>T