Canonical Allele Identifier: PA070905
Gene: MYPN HGNC NCBI

Linked Data

ClinVar Variation Id: 222748
ClinVar RCV Id: RCV000208333 RCV000618176 RCV000691793 RCV001589099 RCV002485363
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_115967.2:p.Gly253Arg
CA070868
NM_032578.4:c.757G>C
CA377105049
NM_032578.4:c.757G>A