ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA2826586497
Gene: MSH6
HGNC
NCBI
Linked Data
ClinVar Variation Id:
2806770
ClinVar RCV Id:
RCV003760747
RCV004371637
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Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001268423.1:p.Ser977Ile
CA346761284
NM_001281494.2:c.2930G>T