Canonical Allele Identifier: PA913197922
Gene: COCH HGNC NCBI

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004077.1:p.Phe59Leu
CA7142945
NM_004086.3:c.177C>A
CA389344115
NM_004086.3:c.175T>C
CA389344120
NM_004086.3:c.177C>G