Canonical Allele Identifier: PA2826637376
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 419599
ClinVar RCV Id: RCV000479350 RCV001037784 RCV001019454
ClinVar Variation Id: 632908
ClinVar RCV Id: RCV000780482 RCV001525394
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Thr783Ser
CA070494
NM_001281494.2:c.2348C>G
CA1649450
NM_001281494.2:c.2347A>T