Canonical Allele Identifier: PA2826627116
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1049172
ClinVar RCV Id: RCV001354922 RCV003298556
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Thr634Ser
CA10654940
NM_001281492.2:c.1901C>G
CA346752960
NM_001281492.2:c.1900A>T