Canonical Allele Identifier: PA2826632817
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 127582
ClinVar RCV Id: RCV000168205 RCV000567226 RCV000656897 RCV000662609 RCV003997247
ClinVar Variation Id: 1729213
ClinVar RCV Id: RCV002324752
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Val776Leu
CA012092
NM_001281493.2:c.2326G>C
CA346758051
NM_001281493.2:c.2326G>T