Allele Registry

Canonical Allele Identifier: PA2573189493

Gene: MYPN HGNC NCBI

ClinVar Allele:

1437529

ClinVar RCV:

RCV001894984

ClinVar Variation:

1369823

HGVS (amino-acid)	Matching Registered Transcripts
NP_001243197.1:p.His835Asn	CA208226042 NM_001256268.2:c.2503C>A