Canonical Allele Identifier: PA645465507
Gene: IFT140 HGNC NCBI

Linked Data

ClinVar Variation Id: 318039
ClinVar RCV Id: RCV000336264 RCV001699311 RCV003888740
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055529.2:p.Gly1027Arg
CA7813325
NM_014714.4:c.3079G>A
CA7813326
NM_014714.4:c.3079G>C