Canonical Allele Identifier: PA3066526654
Gene: CHRND HGNC NCBI

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000742.1:p.Trp78Cys
CA350997343
NM_000751.2:c.234G>C
CA350997344
NM_000751.2:c.234G>T