Canonical Allele Identifier: PA2826724643
Gene: RSPH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 454952

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001273435.1:p.Met224Thr
CA10043746
NM_001286506.2:c.671T>C