Canonical Allele Identifier: PA2826626696
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 134853
ClinVar RCV Id: RCV000121580 RCV000199087 RCV000663104 RCV000774599 RCV001775599
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Glu535Asp
CA009522
NM_001281492.2:c.1605G>C
CA346750656
NM_001281492.2:c.1605G>T