Canonical Allele Identifier: PA2826632805
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 428337
ClinVar RCV Id: RCV000491655 RCV000504512 RCV000759862 RCV000629920
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Arg774Gly
CA070417
NM_001281493.2:c.2320C>G