Canonical Allele Identifier: PA658818391
Gene: MYPN HGNC NCBI

Linked Data

ClinVar Variation Id: 518889
ClinVar RCV Id: RCV000861131 RCV000621402 RCV001293105
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_115967.2:p.Ser1056Phe
CA5522980
NM_032578.4:c.3167C>T