Canonical Allele Identifier: PA2826631620
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 937862
ClinVar RCV Id: RCV001206973
ClinVar Variation Id: 1171586
ClinVar RCV Id: RCV001524801
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Met497Ile
CA346753896
NM_001281493.2:c.1491G>A
CA346753900
NM_001281493.2:c.1491G>C
CA346753903
NM_001281493.2:c.1491G>T