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: PA2580180375
Gene: MYPN HGNC NCBI
ClinVar RCV:
RCV004153925
ClinVar Variation:
2299618
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243197.1:p.Val764Ala
CA376858122
NM_001256268.2:c.2291T>C