Canonical Allele Identifier: PA200022
Gene: MYPN HGNC NCBI

Linked Data

ClinVar Variation Id: 31804

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_115967.2:p.Phe628Leu
CA200020
NM_032578.4:c.1884C>G
CA376840620
NM_032578.4:c.1882T>C
CA376840627
NM_032578.4:c.1884C>A