Canonical Allele Identifier: PA2826630754
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 237144
ClinVar RCV Id: RCV000228803 RCV000506097 RCV001013122
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Gly297Arg
CA068155
NM_001281493.2:c.889G>C
CA346749314
NM_001281493.2:c.889G>A