Canonical Allele Identifier: PA279849
Gene: MEST HGNC NCBI

Linked Data

ClinVar Variation Id: 208394
ClinVar RCV Id: RCV000202328

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002393.2:p.Pro187Ser
CA279847
NM_002402.4:c.559C>T