ClinGen Allele Registry
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Canonical Allele Identifier:
PA163502
Gene: MSH6
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar Allele:
94660
ClinVar RCV:
RCV000128873
RCV000214282
RCV000791437
RCV002288560
RCV003460660
ClinVar Variation:
89186
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000170.1:p.Leu435Pro
CA008468
NM_000179.3:c.1304T>C