Canonical Allele Identifier: PA645507107
Gene: MYPN HGNC NCBI

Linked Data

ClinVar Variation Id: 431886
ClinVar RCV Id: RCV000555234 RCV000764910 RCV000852612 RCV001704650 RCV002323861
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_115967.2:p.Met1035Val
CA5522949
NM_032578.4:c.3103A>G