Canonical Allele Identifier: PA2826630233
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 3230500
ClinVar RCV Id: RCV004520651
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Tyr176Ser
CA346745512
NM_001281493.2:c.527A>C