Canonical Allele Identifier: PA2826630689
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 89220
ClinVar RCV Id: RCV000074683 RCV000219463 RCV000491054 RCV001290557 RCV000791380 RCV003128136 RCV003450930 RCV004537273
ClinVar Variation Id: 1779438
ClinVar RCV Id: RCV002401594
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Leu283Pro
CA009121
NM_001281493.2:c.848T>C
CA2580067689
NM_001281493.2:c.848_849delinsCT