Canonical Allele Identifier: PA2826635984
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 935359
ClinVar RCV Id: RCV001203930 RCV002307698 RCV004010633
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Val460Ile
CA346752910
NM_001281494.2:c.1378G>A