Canonical Allele Identifier: PA2829864908
Gene: CABP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 3136247
ClinVar RCV Id: RCV004432112

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_057450.2:p.Met113Ile
CA6142497
NM_016366.3:c.339G>A
CA6142498
NM_016366.3:c.339G>C
CA381515573
NM_016366.3:c.339G>T