Canonical Allele Identifier: PA645383610
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 237182
ClinVar RCV Id: RCV001368829
ClinVar Variation Id: 410497
ClinVar RCV Id: RCV000464681 RCV000483362 RCV000491614 RCV000662364 RCV001354888 RCV004001848
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Gly1069Arg
CA070372
NM_000179.3:c.3205G>C
CA10582082
NM_000179.3:c.3205G>A