Canonical Allele Identifier: PA2826630435
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 185151
ClinVar RCV Id: RCV000164520 RCV000204361 RCV003235082 RCV003462137 RCV003995346
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Gly227Val
CA008825
NM_001281493.2:c.680G>T