Canonical Allele Identifier: PA2830087316
Gene: MYPN HGNC NCBI

Linked Data

ClinVar Variation Id: 847305
ClinVar RCV Id: RCV001050828
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_115967.2:p.Gly1291Arg
CA376830086
NM_032578.4:c.3871G>A
CA376830087
NM_032578.4:c.3871G>C