Allele Registry

Canonical Allele Identifier: PA2826379501

Gene: MYPN HGNC NCBI

ClinVar Allele:

2019721

ClinVar RCV:

RCV002710339

ClinVar Variation:

1959587

HGVS (amino-acid)	Matching Registered Transcripts
NP_001243196.1:p.Pro1101Ser	CA376858907 NM_001256267.2:c.3301C>T