Allele Registry

Canonical Allele Identifier: PA2830086721

Gene: MYPN HGNC NCBI

ClinVar Allele:

2019721

ClinVar RCV:

RCV002710339

ClinVar Variation:

1959587

HGVS (amino-acid)	Matching Registered Transcripts
NP_115967.2:p.Pro1101Ser	CA376858907 NM_032578.4:c.3301C>T