Allele Registry

Canonical Allele Identifier: PA3057298760

Gene: MYPN HGNC NCBI

ClinVar RCV:

RCV004646042

ClinVar Variation:

3298136

HGVS (amino-acid)	Matching Registered Transcripts
NP_115967.2:p.Thr1105Ile	CA5523021 NM_032578.4:c.3314C>T