Canonical Allele Identifier: PA2826363840
Gene: MEST HGNC NCBI

Linked Data

ClinVar Variation Id: 208394
ClinVar RCV Id: RCV000202328
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001240830.1:p.Pro178Ser
CA279847
NM_001253901.1:c.532C>T