Canonical Allele Identifier: PA2826636008
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_001268423.1:p.Thr465Ser
CA068780
NM_001281494.2:c.1393A>T
CA068793
NM_001281494.2:c.1394C>G