Canonical Allele Identifier: PA2826625115
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 89573
ClinVar RCV Id: RCV000075042 RCV000115445 RCV000212636 RCV000410872 RCV000512927 RCV000524217
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Lys165Arg
CA016588
NM_001281492.2:c.494A>G