ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA913192046
Gene: MSH6
HGNC
NCBI
Linked Data
ClinVar Variation Id:
632905
ClinVar RCV Id:
RCV000780472
RCV001856186
RCV002458395
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Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000170.1:p.Pro12Leu
CA46687631
NM_000179.3:c.35C>T