Canonical Allele Identifier: PA1139690868
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 951839
ClinVar RCV Id: RCV001223834
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Val890Ala
CA346760502
NM_001281494.2:c.2669T>C