Canonical Allele Identifier: PA2826379087
Gene: MYPN HGNC NCBI

Linked Data

ClinVar Variation Id: 684786
ClinVar RCV Id: RCV000845330

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243196.1:p.Thr620Ser
CA376840491
NM_001256267.2:c.1858A>T
CA376840505
NM_001256267.2:c.1859C>G