ClinGen Allele Registry
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Canonical Allele Identifier:
PA299429
Gene: MSH6
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar Allele:
180056
ClinVar RCV:
RCV000160665
RCV000206352
RCV000565934
RCV000656894
RCV000662428
RCV000708864
RCV001030492
RCV002484997
ClinVar Variation:
182620
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000170.1:p.Tyr397Cys
CA008291
NM_000179.3:c.1190A>G