Canonical Allele Identifier: PA2826363825
Gene: MEST HGNC NCBI

Linked Data

ClinVar Variation Id: 208394
ClinVar RCV Id: RCV000202328

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001240829.1:p.Pro173Ser
CA279847
NM_001253900.1:c.517C>T