Canonical Allele Identifier: PA2826633707
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1719480
ClinVar RCV Id: RCV002303753
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Val969Leu
CA072180
NM_001281493.2:c.2905G>C
CA346761229
NM_001281493.2:c.2905G>T