Canonical Allele Identifier: PA2826379440
Gene: MYPN HGNC NCBI

Linked Data

ClinVar Variation Id: 544042
ClinVar RCV Id: RCV000655047

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243196.1:p.Val1036Ala
CA376857437
NM_001256267.2:c.3107T>C