Canonical Allele Identifier: PA2826632217
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 821836
ClinVar RCV Id: RCV001016655 RCV001210150
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Tyr635Cys
CA346755624
NM_001281493.2:c.1904A>G