Canonical Allele Identifier: PA2826379960
Gene: MYPN HGNC NCBI

Linked Data

ClinVar Variation Id: 1359839

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243197.1:p.Pro346Ser
CA208193013
NM_001256268.2:c.1036C>T