Canonical Allele Identifier: PA916012325
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 231365
ClinVar RCV Id: RCV000216678 RCV000708893 RCV000704640 RCV001358640 RCV003469028
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Glu979Gln
CA10578163
NM_001281494.2:c.2935G>C