Canonical Allele Identifier: PA2826636867
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 821928
ClinVar RCV Id: RCV001016842 RCV002550823
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Thr664Ser
CA346756091
NM_001281494.2:c.1990A>T
CA346756094
NM_001281494.2:c.1991C>G