Canonical Allele Identifier: PA2826379680
Gene: MYPN HGNC NCBI

Linked Data

ClinVar Variation Id: 847305
ClinVar RCV Id: RCV001050828
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243196.1:p.Gly1291Arg
CA376830086
NM_001256267.2:c.3871G>A
CA376830087
NM_001256267.2:c.3871G>C