Canonical Allele Identifier: PA2826635838
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 127569
ClinVar RCV Id: RCV000115388 RCV000204867 RCV000212660 RCV001798329 RCV000781575 RCV000986720
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Ile423Val
CA009801
NM_001281494.2:c.1267A>G