ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA216777
Gene: KRT5
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000056634
RCV000250318
RCV000327778
ClinVar Variation:
66275
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000415.2:p.Asp197Glu
CA216776
NM_000424.4:c.591C>A
CA6582796
NM_000424.4:c.591C>G