Canonical Allele Identifier: PA658802500
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 525734
ClinVar RCV Id: RCV000629978
ClinVar Variation Id: 823848
ClinVar RCV Id: RCV001020447
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Arg1166Ser
CA346760164
NM_000179.3:c.3498G>C
CA346760165
NM_000179.3:c.3498G>T