Canonical Allele Identifier: PA2826379949
Gene: MYPN HGNC NCBI

Linked Data

ClinVar Variation Id: 31804
ClinVar RCV Id: RCV000024497 RCV000172766 RCV000252462 RCV001079911 RCV001778668
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243197.1:p.Phe334Leu
CA200020
NM_001256268.2:c.1002C>G
CA376840620
NM_001256268.2:c.1000T>C
CA376840627
NM_001256268.2:c.1002C>A