Canonical Allele Identifier: PA163780
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 140866
ClinVar RCV Id: RCV000129081 RCV000230170 RCV000485282 RCV000663091 RCV001034637 RCV003460886 RCV003997478
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Arg1242His
CA014077
NM_000179.3:c.3725G>A