Canonical Allele Identifier: PA2826629572
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 237217
ClinVar RCV Id: RCV001337476 RCV002378964 RCV003998734
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Pro18Ser
CA10582042
NM_001281493.2:c.52C>T