Canonical Allele Identifier: PA2826379110
Gene: MYPN HGNC NCBI

Linked Data

ClinVar Variation Id: 1359839

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243196.1:p.Pro640Ser
CA208193013
NM_001256267.2:c.1918C>T