Canonical Allele Identifier: PA645476290
Gene: MYMK HGNC NCBI

Linked Data

ClinVar Variation Id: 430839

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073952.1:p.Pro91Thr
CA5312268
NM_001080483.3:c.271C>A