Canonical Allele Identifier: PA2741815937
Gene: KRT17 HGNC NCBI

Linked Data

ClinVar Variation Id: 3014919
ClinVar RCV Id: RCV003878542
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000413.1:p.Thr51Ala
CA8563833
NM_000422.3:c.151A>G
CA2740095338
NM_000422.3:c.150_151delinsTG