Canonical Allele Identifier: PA2826634021
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 230130
ClinVar RCV Id: RCV000215262 RCV000485930 RCV000697066 RCV003462423 RCV003997805
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Lys1023Met
CA10578172
NM_001281493.2:c.3068A>T