Canonical Allele Identifier: PA2826629842
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 89176
ClinVar RCV Id: RCV000162700 RCV000213163 RCV000411429 RCV000627690 RCV001255541 RCV003460658 RCV003997063
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.His80Tyr
CA008133
NM_001281493.2:c.238C>T