Canonical Allele Identifier: PA2826379695
Gene: MYPN HGNC NCBI

Linked Data

ClinVar Variation Id: 969327
ClinVar RCV Id: RCV001244649 RCV004034800
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243196.1:p.Met1305Ile
CA376830326
NM_001256267.2:c.3915G>A
CA376830327
NM_001256267.2:c.3915G>C
CA376830328
NM_001256267.2:c.3915G>T