ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA916010980
Gene: MSH6
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000581415
ClinVar Variation:
491868
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001268421.1:p.Gly39Val
CA346734861
NM_001281492.2:c.116G>T