Canonical Allele Identifier: PA2826637473
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 2869771
ClinVar RCV Id: RCV004011732 RCV003759431
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Asp804Glu
CA346758655
NM_001281494.2:c.2412T>A
CA346758658
NM_001281494.2:c.2412T>G