Canonical Allele Identifier: PA2826636588
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1008737
ClinVar RCV Id: RCV001306118 RCV002437041
ClinVar Variation Id: 2866960
ClinVar RCV Id: RCV003759401
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Phe600Leu
CA346755323
NM_001281494.2:c.1798T>C
CA346755329
NM_001281494.2:c.1800T>A
CA346755330
NM_001281494.2:c.1800T>G