Canonical Allele Identifier: PA645381867
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 419197
ClinVar RCV Id: RCV000542142 RCV000662407 RCV000580933 RCV000765686 RCV001284514 RCV004002290
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Thr767Ser
CA068780
NM_000179.3:c.2299A>T
CA068793
NM_000179.3:c.2300C>G