Canonical Allele Identifier: PA351669
Gene: COL4A5 HGNC NCBI

Linked Data

ClinVar Variation Id: 222061
ClinVar RCV Id: RCV000207631

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000486.1:p.Ala28Ser
CA351668
NM_000495.4:c.82G>T