Canonical Allele Identifier: PA112496
Gene: MYPN HGNC NCBI

Linked Data

ClinVar Variation Id: 31791
ClinVar RCV Id: RCV000024484 RCV000043541 RCV000043542 RCV000157384 RCV000250407 RCV000183595 RCV000852613
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243196.1:p.Pro1112Leu
CA143763
NM_001256267.2:c.3335C>T