Canonical Allele Identifier: PA1139689165
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 920371
ClinVar RCV Id: RCV001179054 RCV001192424 RCV002558898 RCV004006531
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Lys13Gln
CA46687657
NM_001281492.2:c.37A>C