Canonical Allele Identifier: PA2826628757
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 89443
ClinVar RCV Id: RCV000160696 RCV000212686 RCV000410774 RCV000524182 RCV000780485 RCV001354592 RCV003153344 RCV003460688 RCV003997095
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Thr1095Met
CA013768
NM_001281492.2:c.3284C>T