Canonical Allele Identifier: PA2826379966
Gene: MYPN HGNC NCBI

Linked Data

ClinVar Variation Id: 2254691
ClinVar RCV Id: RCV004110423
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243197.1:p.Glu354Asp
CA5522687
NM_001256268.2:c.1062G>C
CA376841012
NM_001256268.2:c.1062G>T