Canonical Allele Identifier: PA2826629564
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 188357
ClinVar RCV Id: RCV000168389 RCV000220509 RCV000656996 RCV003995626 RCV003316071
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Thr17Met
CA016673
NM_001281493.2:c.50C>T