Canonical Allele Identifier: PA916010954
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 182654
ClinVar RCV Id: RCV000160708 RCV000490935 RCV001043688 RCV003320579 RCV003998509
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Arg33Cys
CA016738
NM_001281492.2:c.97C>T