Canonical Allele Identifier: PA658674921
Gene: MYPN HGNC NCBI

Linked Data

ClinVar Variation Id: 488162

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_115967.2:p.Pro269Leu
CA377105146
NM_032578.4:c.806C>T