Canonical Allele Identifier: PA2826626585
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 185463
ClinVar RCV Id: RCV000164891 RCV000200231 RCV000480270 RCV000524126 RCV000781602 RCV001094683 RCV003462152 RCV004528912
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Glu509Lys
CA009445
NM_001281492.2:c.1525G>A