Canonical Allele Identifier: PA2826636177
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 182661
ClinVar RCV Id: RCV000160717 RCV000409643 RCV000570608 RCV000629702 RCV001354913 RCV001582637 RCV003998511
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Ser504Cys
CA010210
NM_001281494.2:c.1511C>G