This is a test version of the ClinGen Allele Registry and hosts obsolete or unreal identifiers. Please visit here for the production version.
Canonical Allele Identifier: PA2830086785
Gene: MYPN HGNC NCBI
ClinVar RCV:
RCV004519880
ClinVar Variation:
3228170
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_115967.2:p.Gln1138Leu
CA376859272
NM_032578.4:c.3413A>T