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: PA2830086638
Gene: MYPN HGNC NCBI
ClinVar RCV:
RCV004153925
ClinVar Variation:
2299618
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_115967.2:p.Val1058Ala
CA376858122
NM_032578.4:c.3173T>C