Canonical Allele Identifier: PA2826637546
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 410420
ClinVar RCV Id: RCV000467819 RCV000773186 RCV000662840 RCV001805074 RCV004001824
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Gln820Glu
CA16611045
NM_001281494.2:c.2458C>G