Canonical Allele Identifier: PA2826636021
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 421501
ClinVar RCV Id: RCV000481556 RCV001190572 RCV000822224 RCV003470572 RCV004003355
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Pro466Ala
CA068796
NM_001281494.2:c.1396C>G