Canonical Allele Identifier: PA658818329
Gene: MYPN HGNC NCBI

Linked Data

ClinVar Variation Id: 520317
ClinVar RCV Id: RCV000618459 RCV001231665
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_115967.2:p.Ser627Thr
CA376840605
NM_032578.4:c.1879T>A