Canonical Allele Identifier: PA2826633172
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 142773
ClinVar RCV Id: RCV000132174 RCV000541079 RCV001267890 RCV001174713 RCV002514752 RCV003462035
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Gly855Cys
CA012982
NM_001281493.2:c.2563G>T