Canonical Allele Identifier: PA2826625017
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 127605
ClinVar RCV Id: RCV000115443 RCV000212634 RCV000685169 RCV003997256
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Gly143Arg
CA016493
NM_001281492.2:c.427G>A
CA346740406
NM_001281492.2:c.427G>C