Canonical Allele Identifier: PA2826636189
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 655766
ClinVar RCV Id: RCV000812013 RCV001257480 RCV002453838
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Val507Ala
CA069038
NM_001281494.2:c.1520T>C