Canonical Allele Identifier: PA1139687461
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_001243197.1:p.Gly997Arg
CA376830086
NM_001256268.2:c.2989G>A
CA376830087
NM_001256268.2:c.2989G>C