Canonical Allele Identifier: PA2826635831
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 418875
ClinVar RCV Id: RCV000484115 RCV001014624 RCV001851150
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Gly421Arg
CA16617669
NM_001281494.2:c.1261G>C