Allele Registry

Canonical Allele Identifier: PA3057257086

Gene: MYPN HGNC NCBI

ClinVar RCV:

RCV004592411

ClinVar Variation:

3253446

HGVS (amino-acid)	Matching Registered Transcripts
NP_115967.2:p.Leu1108Phe	CA5523023 NM_032578.4:c.3322C>T