Canonical Allele Identifier: PA2826379958
Gene: MYPN HGNC NCBI

Linked Data

ClinVar Variation Id: 520319
ClinVar RCV Id: RCV000618653 RCV000655054 RCV001584445 RCV003945566
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243197.1:p.Gly340Arg
CA5522679
NM_001256268.2:c.1018G>A
CA376840711
NM_001256268.2:c.1018G>C