Canonical Allele Identifier: PA164743
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 141197
ClinVar RCV Id: RCV000129593 RCV000705750 RCV001293976 RCV003460897
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Glu1052Gly
CA011668
NM_000179.3:c.3155A>G