Canonical Allele Identifier: PA123779
Gene: MPL HGNC NCBI

Linked Data

ClinVar Variation Id: 14157

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005364.1:p.Pro635Leu
CA123777
NM_005373.3:c.1904C>T