Canonical Allele Identifier: PA103882
Gene: KRT6A HGNC NCBI

Linked Data

ClinVar Variation Id: 66585
ClinVar RCV Id: RCV000057007 RCV000128818
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005545.1:p.Asn171Asp
CA217351
NM_005554.4:c.511A>G