Canonical Allele Identifier: PA2826633269
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 428335
ClinVar RCV Id: RCV000491443 RCV001303894 RCV003464047 RCV003237881
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Gly876Asp
CA071129
NM_001281493.2:c.2627G>A