Canonical Allele Identifier: PA160889
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 134848
ClinVar RCV Id: RCV000121571 RCV000215694 RCV000457237 RCV000586380 RCV003997351 RCV003460854
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Ala159Val
CA015692
NM_000179.3:c.476C>T