Canonical Allele Identifier: PA335327
Gene: MYPN HGNC NCBI

Linked Data

ClinVar Variation Id: 201892
ClinVar RCV Id: RCV001344879 RCV002453665
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_115967.2:p.Leu1132Phe
CA335325
NM_032578.4:c.3394C>T