ClinGen Allele Registry
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Canonical Allele Identifier:
PA2826632021
Gene: MSH6
HGNC
NCBI
Linked Data
ClinVar Variation Id:
439203
ClinVar RCV Id:
RCV000506119
RCV000794150
RCV001179711
RCV004003551
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001268422.1:p.Leu591Val
CA069423
NM_001281493.2:c.1771C>G