ClinGen Allele Registry
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Canonical Allele Identifier:
PA645381867
Gene: MSH6
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar Allele:
405897
ClinVar RCV:
RCV000542142
RCV000580933
RCV000662407
RCV000765686
RCV001284514
RCV004002290
ClinVar Variation:
419197
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000170.1:p.Thr767Ser
CA068780
NM_000179.3:c.2299A>T
CA068793
NM_000179.3:c.2300C>G