Canonical Allele Identifier: PA2826633173
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 89393
ClinVar RCV Id: RCV000131534 RCV000202300 RCV002513797 RCV002510780 RCV003450969 RCV004555853
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Gly855Ser
CA012971
NM_001281493.2:c.2563G>A