ClinGen Allele Registry
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Canonical Allele Identifier:
PA645381881
Gene: MSH6
HGNC
NCBI
Linked Data
ClinVar Variation Id:
421501
ClinVar RCV Id:
RCV000481556
RCV001190572
RCV000822224
RCV003470572
RCV004003355
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000170.1:p.Pro768Ala
CA068796
NM_000179.3:c.2302C>G