Canonical Allele Identifier: PA2826379443
Gene: MYPN HGNC NCBI

Linked Data

ClinVar Variation Id: 2103470
ClinVar RCV Id: RCV003022165
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243196.1:p.Leu1039Trp
CA376857499
NM_001256267.2:c.3116T>G