Canonical Allele Identifier: PA916012018
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_001268423.1:p.Ser883Ala
CA013340
NM_001281494.2:c.2647T>G