Canonical Allele Identifier: PA2826630657
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 234864
ClinVar RCV Id: RCV000223441 RCV000555846 RCV000564916 RCV000766399 RCV003469114 RCV003998645
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Arg275Gly
CA068077
NM_001281493.2:c.823C>G