Canonical Allele Identifier: PA2826631767
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 231561
ClinVar RCV Id: RCV000217167 RCV000985833 RCV002247652 RCV003462469 RCV003997908 RCV000461932
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Ser532Asn
CA069123
NM_001281493.2:c.1595G>A