Canonical Allele Identifier: PA101452
Gene: HCFC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 39695

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005325.2:p.Ser225Asn
CA130460
NM_005334.3:c.674G>A