Canonical Allele Identifier: PA2826179208
Gene: RSPH9 HGNC NCBI

Linked Data

ClinVar Variation Id: 357016
ClinVar RCV Id: RCV000401748 RCV000732669 RCV001095287
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001180270.1:p.Met92Ile
CA3828266
NM_001193341.2:c.276G>A
CA364288493
NM_001193341.2:c.276G>C
CA364288495
NM_001193341.2:c.276G>T