Canonical Allele Identifier: PA2826379932
Gene: MYPN HGNC NCBI

Linked Data

ClinVar Variation Id: 3228157
ClinVar RCV Id: RCV004519867
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243197.1:p.Ala321Thr
CA376840431
NM_001256268.2:c.961G>A