Canonical Allele Identifier: PA2826635691
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1319500
ClinVar RCV Id: RCV002540732 RCV003237501
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Tyr388Cys
CA346750795
NM_001281494.2:c.1163A>G