Canonical Allele Identifier: PA2826635391
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 230869
ClinVar RCV Id: RCV000219912 RCV000233003 RCV000484834 RCV000662524 RCV000657004 RCV003469017 RCV003997865
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Gly322Ser
CA10578081
NM_001281494.2:c.964G>A