Canonical Allele Identifier: PA916011004
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 216296
ClinVar RCV Id: RCV000197947 RCV000575386 RCV000765677 RCV003996993
ClinVar Variation Id: 219577
ClinVar RCV Id: RCV000204112 RCV000484712 RCV000561391 RCV000663157 RCV000765676 RCV003997571
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Gly46Arg
CA337552
NM_001281492.2:c.136G>C
CA348361
NM_001281492.2:c.136G>A