ClinGen Allele Registry
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Canonical Allele Identifier:
PA338865
Gene: MSH6
HGNC
NCBI
Linked Data
ClinVar Variation Id:
216310
ClinVar RCV Id:
RCV000199786
RCV000215044
RCV001194335
RCV003996999
RCV003491941
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000170.1:p.Arg1034Gln
CA070049
NM_000179.3:c.3101G>A