Canonical Allele Identifier: PA194159
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 186209
ClinVar RCV Id: RCV000165760 RCV000703941 RCV001544988 RCV003995453
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Ser1185Ala
CA013340
NM_000179.3:c.3553T>G