Canonical Allele Identifier: PA2826379973
Gene: MYPN HGNC NCBI

Linked Data

ClinVar Variation Id: 1387825
ClinVar RCV Id: RCV001908230

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243197.1:p.Pro362Ser
CA208193114
NM_001256268.2:c.1084C>T