Canonical Allele Identifier: PA2826630172
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 578073
ClinVar RCV Id: RCV000700974 RCV003165866
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Pro160Leu
CA346745042
NM_001281493.2:c.479C>T