Canonical Allele Identifier: PA916012022
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 410454
ClinVar RCV Id: RCV000775741 RCV000465628 RCV004001834
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Gly884Arg
CA16610969
NM_001281494.2:c.2650G>C