Canonical Allele Identifier: PA2826635953
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 182634
ClinVar RCV Id: RCV000160679 RCV000821022 RCV000772630 RCV003998496
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Thr452Pro
CA009921
NM_001281494.2:c.1354A>C