Canonical Allele Identifier: PA2826635869
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 234747
ClinVar RCV Id: RCV000223534 RCV000532996 RCV000564357 RCV000758666
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Arg430Gln
CA068599
NM_001281494.2:c.1289G>A