ClinGen Allele Registry
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Canonical Allele Identifier:
PA2826636008
Gene: MSH6
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar Allele:
405897
ClinVar RCV:
RCV000542142
RCV000580933
RCV000662407
RCV000765686
RCV001284514
RCV004002290
ClinVar Variation:
419197
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001268423.1:p.Thr465Ser
CA068780
NM_001281494.2:c.1393A>T
CA068793
NM_001281494.2:c.1394C>G