Canonical Allele Identifier: PA2826636450
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 418649
ClinVar RCV Id: RCV000487290 RCV000552497 RCV000567884 RCV003470530 RCV004002264
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Ile570Thr
CA16617678
NM_001281494.2:c.1709T>C