Canonical Allele Identifier: PA2826632219
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 525744
ClinVar RCV Id: RCV000630002 RCV002438641
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Asp636His
CA346755629
NM_001281493.2:c.1906G>C