Canonical Allele Identifier: PA2826634301
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 823445
ClinVar RCV Id: RCV001019694 RCV001037488 RCV002466602 RCV004004589
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Gln23Glu
CA346740972
NM_001281494.2:c.67C>G