Canonical Allele Identifier: PA2826379502
Gene: MYPN HGNC NCBI

Linked Data

ClinVar Variation Id: 544043
ClinVar RCV Id: RCV000655048 RCV002499130
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243196.1:p.Pro1101Thr
CA376858903
NM_001256267.2:c.3301C>A