Allele Registry

Canonical Allele Identifier: PA3057387803

Gene: MYPN HGNC NCBI

ClinVar RCV:

RCV004987467

ClinVar Variation:

3402069

HGVS (amino-acid)	Matching Registered Transcripts
NP_115967.2:p.Asn1109Ser	CA376858989 NM_032578.4:c.3326A>G