Canonical Allele Identifier: PA2741997019
Gene: MYPN HGNC NCBI

Linked Data

ClinVar Variation Id: 2563976
ClinVar RCV Id: RCV003306305

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_115967.2:p.Gly616Val
CA208192861
NM_032578.4:c.1847G>T