Canonical Allele Identifier: PA2828434351
Gene: ABCC11 HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357425.1:p.Val491Ile
CA8043868
NM_001370496.1:c.1471G>A