Canonical Allele Identifier: PA105920
Gene: KRT2 HGNC NCBI
ClinVar RCV:
RCV000009900
ClinVar Variation:
9315
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000414.2:p.Asn186Asp
CA120296
NM_000423.3:c.556A>G