Canonical Allele Identifier: PA2826637393
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 89362
ClinVar RCV Id: RCV000074829 RCV000160725 RCV000524164 RCV000586012 RCV000764430 RCV003149721
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Pro785Arg
CA012273
NM_001281494.2:c.2354C>G