Canonical Allele Identifier: PA2573290906
Gene: MYPN HGNC NCBI

Linked Data

ClinVar Variation Id: 1387825
ClinVar RCV Id: RCV001908230

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_115967.2:p.Pro656Ser
CA208193114
NM_032578.4:c.1966C>T