Canonical Allele Identifier: PA645468807
Gene: KRT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 309623
ClinVar RCV Id: RCV000320436 RCV001636880
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000414.2:p.Ser101Gly
CA6585888
NM_000423.3:c.301A>G