Canonical Allele Identifier: PA2826636174
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 847677
ClinVar RCV Id: RCV001051274 RCV003307860
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Ser504Thr
CA346754000
NM_001281494.2:c.1510T>A