Canonical Allele Identifier: PA2741816396
Gene: KRT14 HGNC NCBI

Linked Data

ClinVar Variation Id: 2763642
ClinVar RCV Id: RCV003565199
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000517.3:p.Asp226Glu
CA8562640
NM_000526.5:c.678C>G
CA399478287
NM_000526.5:c.678C>A