Canonical Allele Identifier: PA2742022559
Gene: TMEM171 HGNC NCBI
ClinVar RCV:
RCV004282599
ClinVar Variation:
2512422
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_775761.4:p.Ile41Phe
CA3302540
NM_173490.8:c.121A>T