Canonical Allele Identifier: PA191189
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 185159
ClinVar RCV Id: RCV000164528 RCV000205577 RCV000662485 RCV001580460 RCV003462138 RCV002271437
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Met875Thr
CA010617
NM_000179.3:c.2624T>C