Canonical Allele Identifier: PA2826634290
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 483793
ClinVar RCV Id: RCV000562475 RCV000821409 RCV004530608
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Thr21Ser
CA346740928
NM_001281494.2:c.61A>T
CA346740931
NM_001281494.2:c.62C>G