Canonical Allele Identifier: PA915965645
Gene: KRT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 779152
ClinVar RCV Id: RCV000959926 RCV001111993
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000414.2:p.Arg34Trp
CA6585969
NM_000423.3:c.100C>T