Canonical Allele Identifier: PA2826632857
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 230897
ClinVar RCV Id: RCV000223078 RCV000699366 RCV003997868
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Pro784Arg
CA070524
NM_001281493.2:c.2351C>G