Canonical Allele Identifier: PA916011811
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 127555
ClinVar RCV Id: RCV000552028 RCV000570684 RCV000758608 RCV000985821 RCV002267855
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Asp88Asn
CA008202
NM_001281494.2:c.262G>A