Canonical Allele Identifier: PA166701
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 141885
ClinVar RCV Id: RCV000130582 RCV000530606 RCV000484580 RCV000986696 RCV002281956 RCV003998065
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Pro12Thr
CA013137
NM_000179.3:c.34C>A