Canonical Allele Identifier: PA645378221
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 410476
ClinVar RCV Id: RCV000459919 RCV000481267 RCV000567789 RCV000663030 RCV001721501
ClinVar Variation Id: 483766
ClinVar RCV Id: RCV000566299 RCV000805474 RCV001570489
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Gly39Arg
CA067220
NM_000179.3:c.115G>A
CA067226
NM_000179.3:c.115G>C