Canonical Allele Identifier: PA2826634705
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 801217
ClinVar RCV Id: RCV000985823 RCV001180968 RCV001224992
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Ile162Thr
CA346745110
NM_001281494.2:c.485T>C