Canonical Allele Identifier: PA2826379118
Gene: MYPN HGNC NCBI

Linked Data

ClinVar Variation Id: 1015070

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243196.1:p.Pro649Ala
CA5522688
NM_001256267.2:c.1945C>G