Canonical Allele Identifier: PA2826633475
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 490008
ClinVar RCV Id: RCV000579922
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Phe920Leu
CA346760838
NM_001281493.2:c.2758T>C
CA346760843
NM_001281493.2:c.2760T>A
CA346760844
NM_001281493.2:c.2760T>G