Canonical Allele Identifier: PA167690
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 142181
ClinVar RCV Id: RCV000131161 RCV000196009 RCV000409980 RCV000524107 RCV000590712 RCV001355650 RCV002281960
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Asn455Thr
CA008530
NM_000179.3:c.1364A>C