Canonical Allele Identifier: PA279848
Gene: MEST HGNC NCBI

Linked Data

ClinVar Variation Id: 208394
ClinVar RCV Id: RCV000202328

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_803490.1:p.Pro178Ser
CA279847
NM_177524.2:c.532C>T