Canonical Allele Identifier: PA2826625560
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 182620
ClinVar RCV Id: RCV000160665 RCV000206352 RCV000565934 RCV000656894 RCV000662428 RCV000708864 RCV001030492 RCV002484997
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Tyr267Cys
CA008291
NM_001281492.2:c.800A>G