Canonical Allele Identifier: PA2826635206
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 127563
ClinVar RCV Id: RCV000115382 RCV000230963 RCV000235184 RCV000409045 RCV001192457 RCV003460812
ClinVar Variation Id: 2840176
ClinVar RCV Id: RCV003758429
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Phe280Leu
CA009115
NM_001281494.2:c.840T>G
CA346748887
NM_001281494.2:c.838T>C
CA346748902
NM_001281494.2:c.840T>A