Canonical Allele Identifier: PA2826628849
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 232375
ClinVar RCV Id: RCV000218524 RCV001243869 RCV003462494 RCV003322762 RCV003997965
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Arg1112Cys
CA10578156
NM_001281492.2:c.3334C>T