Canonical Allele Identifier: PA2826631003
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 954699
ClinVar RCV Id: RCV001227206 RCV001553683 RCV003584862
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Pro354Leu
CA346750597
NM_001281493.2:c.1061C>T