Canonical Allele Identifier: PA2741813182
Gene: KRT12 HGNC NCBI

Linked Data

ClinVar Variation Id: 3048993
ClinVar RCV Id: RCV003958906
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000214.1:p.Gly54Arg
CA8548948
NM_000223.4:c.160G>A
CA8548949
NM_000223.4:c.160G>C