Canonical Allele Identifier: PA1139689161
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 919074
ClinVar RCV Id: RCV001177000 RCV002295330
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Pro12Arg
CA346734526
NM_001281492.2:c.35C>G