Canonical Allele Identifier: PA2826637440
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 233674
ClinVar RCV Id: RCV000214591 RCV001854702 RCV002472974 RCV003998571
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Cys796Tyr
CA10578139
NM_001281494.2:c.2387G>A